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Ethacrynic acid

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Name

Ethacrynic acid

EINECS 200-384-1
CAS No. 58-54-8 Density 1.35g/cm3
PSA 63.60000 LogP 3.60570
Solubility Soluble in ethanol, chloroform, ether, ammonia, carbonates, and methanol. Insoluble in water. Melting Point 122
Formula C13H12 Cl2 O4 Boiling Point 480°Cat760mmHg
Molecular Weight 303.142 Flash Point 244.1°C
Transport Information N/A Appearance White solid.
Safety Poison by intravenous route. Moderately toxic by ingestion. Human systemic effects by ingestion and intravenous routes: urine volume increase, impaired hearing, and tinnitus (ringing in the ears). A diuretic. When heated to decomposition it emits toxic fumes of Cl. Risk Codes R20/21/22;R36/37/38   
Molecular Structure Molecular Structure of 58-54-8 (Ethacrynic acid) Hazard Symbols
Synonyms

Aceticacid, [2,3-dichloro-4-(2-methylene-1-oxobutyl)phenoxy]- (9CI); Acetic acid,[2,3-dichloro-4-(2-methylenebutyryl)phenoxy]- (8CI);2,3-Dichloro-4-(2-ethyl-1-oxo-2-propenyl)-phenoxyacetic acid; Crinuril;Edecril; Edecrin; Edecrina; Endecril; Etacrynic acid; Etakrinic acid;Ethacrynic acid; Hidromedin; Hydromedin; MK 595; Mingit; NSC 624008; NSC 85791;Otacril; Reomax; Taladren; Uregit;[2,3-Dichloro-4-(2-methylene-1-oxobutyl)phenoxy]acetic acid;[2,3-Dichloro-4-(2-methylenebutyryl)phenoxy]acetic acid;[4-(2-Methylenebutyryl)-2,3-dichlorophenoxy]acetic acid

Article Data 32

Ethacrynic acid Synthetic route

50-00-0

formaldehyd

1217-67-0

<2,3-dichloro-4-(1-oxobutyl)phenyloxy>acetic acid

58-54-8

ethacrynic acid

Conditions
ConditionsYield
With potassium carbonate In ethanol; water at 90℃; for 10h;80.5%

t-butylamine salt of ethacrynic acid

58-54-8

ethacrynic acid

Conditions
ConditionsYield
With hydrogenchloride In water; ethyl acetate at 30℃; for 0.5h; pH=2 - 3;60.1%
4115-00-8

2,3-dichloro-4-(2-methylenebutyryl)-phenol

58-54-8

ethacrynic acid

50-00-0

formaldehyd

2977-51-7

2,3-Dichlor-4-butyryl-phenoxyessigsaeure-aethylester

58-54-8

ethacrynic acid

Conditions
ConditionsYield
Stage #1: formaldehyd; 2,3-Dichlor-4-butyryl-phenoxyessigsaeure-aethylester With potassium carbonate Aldol condensation;
Stage #2: With hydrogenchloride; water
With potassium carbonate In ethanol; water for 24h; Aldol Condensation; Reflux;
2350-46-1

2',3'-dichloro-4'-hydroxybutyrophenone

58-54-8

ethacrynic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: potassium carbonate / toluene / 48 h / Reflux
2: potassium carbonate / ethanol; water / 24 h / Reflux
View Scheme
Multi-step reaction with 2 steps
1.1: potassium carbonate; potassium iodide / acetone / 0.5 h
1.2: 4 h / 60 °C
1.3: 2 h / 20 °C
2.1: potassium carbonate / ethanol; water / 10 h / 90 °C
View Scheme
Multi-step reaction with 4 steps
1.1: potassium carbonate / ethanol / 0.33 h / 30 °C
1.2: 12 h / 30 - 83 °C
2.1: N,N-dimethyl-formamide / 0.17 h / 30 °C
2.2: 12 h / 100 °C
3.1: N,N-dimethyl-formamide; toluene / 5 h / 20 - 30 °C
4.1: hydrogenchloride / ethyl acetate; water / 0.5 h / 30 °C / pH 2 - 3
View Scheme
576-24-9

2,3-dichlorophenol

58-54-8

ethacrynic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: aluminum (III) chloride / carbon disulfide
2: potassium carbonate / toluene / 48 h / Reflux
3: potassium carbonate / ethanol; water / 24 h / Reflux
View Scheme
Multi-step reaction with 4 steps
1.1: potassium carbonate / acetone / 0.5 h
1.2: 3 h / 60 °C
2.1: aluminum (III) chloride / dichloromethane / 3.5 h / 0 - 40 °C
2.2: 3 h / 20 °C / Cooling with ice
3.1: potassium carbonate; potassium iodide / acetone / 0.5 h
3.2: 4 h / 60 °C
3.3: 2 h / 20 °C
4.1: potassium carbonate / ethanol; water / 10 h / 90 °C
View Scheme

Os(η6-p-cymene)(acetylacetonato)(2-(2,3-dichloro-4-(2-ethylenebutanoyl)phenoxy)acetato)

A

[(η6-p-cymene)Os(acetylacetonato)Cl]

B

58-54-8

ethacrynic acid

Conditions
ConditionsYield
In water; dimethyl sulfoxide at 37℃; for 72h;
1984-59-4

2,3-dichloroanisole

58-54-8

ethacrynic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: aluminum (III) chloride / dichloromethane / 3.5 h / 0 - 40 °C
1.2: 3 h / 20 °C / Cooling with ice
2.1: potassium carbonate; potassium iodide / acetone / 0.5 h
2.2: 4 h / 60 °C
2.3: 2 h / 20 °C
3.1: potassium carbonate / ethanol; water / 10 h / 90 °C
View Scheme
Multi-step reaction with 5 steps
1.1: aluminum (III) chloride / dichloromethane / 0.17 h / 30 °C
1.2: 8 h / 20 - 30 °C
1.3: 8 h / 30 - 42 °C
2.1: potassium carbonate / ethanol / 0.33 h / 30 °C
2.2: 12 h / 30 - 83 °C
3.1: N,N-dimethyl-formamide / 0.17 h / 30 °C
3.2: 12 h / 100 °C
4.1: N,N-dimethyl-formamide; toluene / 5 h / 20 - 30 °C
5.1: hydrogenchloride / ethyl acetate; water / 0.5 h / 30 °C / pH 2 - 3
View Scheme

C26H22Cl12Nb2O8

58-54-8

ethacrynic acid

Conditions
ConditionsYield
In diethyl ether; water at 20℃; for 48h; Inert atmosphere;
1217-67-0

<2,3-dichloro-4-(1-oxobutyl)phenyloxy>acetic acid

58-54-8

ethacrynic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: N,N-dimethyl-formamide / 0.17 h / 30 °C
1.2: 12 h / 100 °C
2.1: N,N-dimethyl-formamide; toluene / 5 h / 20 - 30 °C
3.1: hydrogenchloride / ethyl acetate; water / 0.5 h / 30 °C / pH 2 - 3
View Scheme

Ethacrynic acid Chemical Properties

IUPAC Name: 2-[2,3-Dichloro-4-(2-methylidenebutanoyl)phenoxy]acetic acid
Product Name: Ethacrynic acid
The MF of Ethacrynic acid (CAS NO.58-54-8) is C13H12Cl2O4.

                       
The MW of Ethacrynic acid (CAS NO.58-54-8) is 303.14.
Synonyms of Ethacrynic acid (CAS NO.58-54-8): (2,3-Dichloro-4-(2-methylene-1-oxobutyl)phenoxy)-aceticacid ; (2,3-Dichloro-4-(2-methylene-1-oxobutyl)phenoxy)aceticacid ; (4-(2-Methylenebutyryl)-2,3-dichlorophenoxy)aceticacid ; [2,3-Dichloro-4-(2-methylene-1-oxobutyl)phe-noxy]aceticacid ; Crinuryl ; Edecril ; Edecrin
Index of Refraction: 1.558 
Apperance: White solid
EINECS: 200-384-1
Density: 1.35 g/ml
Flash Point: 244.1 °C
Boiling Point: 480 °C
Melting Point: 125 °C
Merck: 3717

Ethacrynic acid Uses

  Ethacrynic acid (CAS NO.58-54-8) is strong diuretic inhibiting renal tubular sodium and chloride re-absorption.The role is strong and fast and a serious edema required for drugs, but the toxicity is large.

Ethacrynic acid Production

Raw materials: Sodium hydroxide-->Hydrochloric acid-->Methanol-->Diethyl ether-->Sulfuric acid -->Acetic acid glacial-->Sodium sulfate-->Sodium bicarbonate-->Benzene-->Aluminium chloride-->Sodium acetate-->Carbon disulphide-->Paraformaldehyde-->Chloroacetic acid-->Cyclohexane-->Ethyl bromoacetate-->Heptane-->Butyryl chloride-->Carbon-->Dimethylamine hydrochloride-->Methylcyclohexane-->2,3-Dichlorophenol-->2,6-Dichloroanisole-->Butyrophenone-->Ethyl phenoxyacetate-->2,3-Dichlorophenoxyacetic Acid

Ethacrynic acid Toxicity Data With Reference

1.    

orl-wmn TDLo:4 mg/kg:EAR

    AIMDAP    Archives of Internal Medicine. 117 (1966),715.
2.    

orl-man TDLo:3 mg/kg:EAR,KID

    AIMDAP    Archives of Internal Medicine. 117 (1966),715.
3.    

ivn-wmn TDLo:3 mg/kg:EAR

    AIMDAP    Archives of Internal Medicine. 117 (1966),715.
4.    

orl-rat LD50:1 g/kg

    YAKUD5    Gekkan Yakuji. Pharmaceuticals Monthly. 21 (1979),775.
5.    

ipr-rat LD50:43 mg/kg

    OYYAA2    Oyo Yakuri. Pharmacometrics. 2 (1968),411.
6.    

orl-mus LD50:627 mg/kg

    MEIEDD    Merck Index. 10 (1983),539.
7.    

ivn-mus LD50:176 mg/kg

    MEIEDD    Merck Index. 10 (1983),539.

Ethacrynic acid Safety Profile

Poison by intravenous route. Moderately toxic by ingestion. Human systemic effects by ingestion and intravenous routes: urine volume increase, impaired hearing, and tinnitus (ringing in the ears). A diuretic. When heated to decomposition it emits toxic fumes of Cl.Safety information of Ethacrynic acid (CAS NO.58-54-8):
Hazard Codes  HarmfulXn
Risk Statements 
20/21/22 Harmful by inhalation, in contact with skin and if swallowed
36/37/38 Irritating to eyes, respiratory system and skin
Safety Statements 
26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
36 Wear suitable protective clothing
WGK Germany  3
RTECS  AG6600000

Ethacrynic acid Specification

 Ethacrynic acid may react vigorously with strong oxidizing agents. Can react exothermically with reducing agents (such as alkali metals and hydrides) to release gaseous hydrogen. May react exothermically with acids. Reacts exothermically with all bases both organic (for example, the amines) and inorganic.

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