37777-71-2

Basic information

• Product Name: 2-(4-CHLORO-2-NITROPHENYL)ACETIC ACID
• Synonyms: (4-CHLORO-2-NITRO-PHENYL)-ACETIC ACID;2-(4-CHLORO-2-NITROPHENYL)ACETIC ACID;4-Chloro-2-Nitrobenzeneaceticacid;Benzeneacetic Acid,4-Chloro-2-Nitro-;Nsc 115143
• CAS NO: 37777-71-2
• Molecular Formula: C₈H₆ClNO₄
• Molecular Weight: 215.591
• Mol File: 37777-71-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 361.2 °C at 760 mmHg
• Flash Point: 172.2 °C
• Appearance: /
• Density: 1.532 g/cm³
• Vapor Pressure: 7.56E-06mmHg at 25°C
• Refractive Index: 1.61
• CAS DataBase Reference: 2-(4-CHLORO-2-NITROPHENYL)ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-CHLORO-2-NITROPHENYL)ACETIC ACID(37777-71-2)
• EPA Substance Registry System: 2-(4-CHLORO-2-NITROPHENYL)ACETIC ACID(37777-71-2)

Safety Data

• Hazardous Substances Data: 37777-71-2(Hazardous Substances Data)

Usage

Preparation

The filtrate of Step A, above, is adjusted to pH 8-9 with 2 N sodium hydroxide and is heated at 35-40 °C. while adding a 3-6% aqueous hydrogen peroxide solu tion until samples no longer turn dark on treatment with 2N sodium hydroxide. The tan precipitate is suspended in 1500 ml. of water, adjusted to pH 8-9 and similarly treated with aqueous hydrogen peroxide. The combined reaction mixtures are then acidified with concentrated hydrochloride acid to obtain a precipitate which are re covered by filtration, washed 3 times with water and dried in vacuo. The crude product (mp 145-150°C) is recrystallized from ether to obtain 4-chloro-2-nitro phenylacetic acid, m.p. 156-159°C.

InChI:InChI=1/C8H6ClNO4/c9-6-2-1-5(3-8(11)12)7(4-6)10(13)14/h1-2,4H,3H2,(H,11,12)

Upstream product

• 7647-01-0 hydrogenchloride 
• 116435-81-5 (4-amino-2-nitrophenyl)acetic acid 
• 89-61-2 2,5-dichloronitrobenzene 
• 147124-32-1 dimethyl (4-chloro-2-nitrophenyl)malonate 
• 643-43-6 (2,4-dinitro-phenyl)-acetic acid 
• 89-59-8 4-chloro-2-nitrotoluene 
• 87081-90-1 (4-chloro-2-nitro-phenyl)-acetonitrile 
• 71300-08-8 (4-chloro-2-nitro-phenyl)-pyruvic acid 
• 95-92-1 oxalic acid diethyl ester 

Downstream Products

• 6127-13-5 1-(4-chloro-2-nitrophenyl)propan-2-one 
• 108274-38-0 4-Chlor-2-nitrophenylessigsaeure-ethylester 
• 35318-51-5 4'-Chlor-2'-nitro-4-trifluormethyl-α-phenylzimtsaeure 
• 56988-30-8 C₁₅H₈Cl₃NO₄ 
• 177985-31-8 (2-amino-4-chlorophenyl)acetic acid 
• 28230-26-4 6-chloro-1-hydroxy-indolin-2-one 
• 56341-37-8 6-chloro-2-oxindole 
• 890532-46-4 glycine, N-[[4-chloro-2-[[7-methoxy-6-[2-[[2-(4-morpholinyl)ethyl]amino]ethoxy]-4-quinazolinyl]amino]phenyl]acetyl]- 
• 1056010-85-5 glycine, N-[[2-[[6-(3-aminopropoxy)-7-methoxy-4-quinazolinyl]amino]-4-chlorophenyl]acetyl]-, ethyl ester 
• 807640-36-4 alanine, N-[[2-[[6-(2-aminoethoxy)-7-methoxy-4-quinazolinyl]amino]-4-chlorophenyl]acetyl]-2-methyl-, ethyl ester 
• 807640-25-1 glycine, N-[[2-[[6-(2-bromoethoxy)-7-methoxy-4-quinazolinyl]amino]-4-chlorophenyl]acetyl]-, ethyl ester 

Relevant articles and documents

Preparation method of ziprasidone intermediate

The invention relates to a preparation method of a ziprasidone intermediate.The preparation method is a method to prepare 6-chloro-2-indolone by one-pot process, an alkali liquid and phase-transfer catalyst low in price are used in the preparation process to substitute the prior art sodium hydride necessary to use and high in price, recyclable low-grade aliphatic ketone and low-grade fatty alcohol are used to substitute DMF (dimethyl formamide) and DMSO (dimethylsulfoxide) difficult to recycle, the cost is reduced greatly, the materials used herein are cheap and easy to obtain, the process is simple and feasible, posttreatment steps are simplified, particularly the step (1) requires no washing, extracting and purifying operation, one step may be performed directly, the whole operating step needs no use of column chromatography for purification, the whole preparation process is simplified, and the method is convenient to industrialize; in the synthetic process of formula III compound, a deacidifying process is mild and safe; in the synthesis of formula II compound, low-valence sulfur-containing compound is used in reduction, generation of mass waste acid liquid is avoided, production is safe and environment-friendly, and the preparation process is simple and easy.

A PROCESS FOR THE PREPARATION OF OXINDOLE DERIVATIVES

A process for the preparation of oxindole derivative of formula (I) comprising reacting compound of formula (II) with dialkyl malonate, COOR1-COOR1, in the presence of a mild base to give compound of formula (III); and wherein R is selected from hydrogen, linear, branched or cyclic alkyl, aryl, substituted aryl, heteroaryl, haloalkyl like CF3, alkoxy, haloalkoxy, thioalkyl and halogen.; R1 is selected from linear, branched and cyclic alkyl (C1 to C4 groups); and X is selected from chloro, bromo, fluoro and iodo groups;further converting compound of formula (III) to compound of formula (I).