(5S)-3-[4-[(3-Chlorophenyl)methoxy]phenyl]-5-(hydroxymethyl)-2-oxazolidinone

Base Information

Chemical Name:(5S)-3-[4-[(3-Chlorophenyl)methoxy]phenyl]-5-(hydroxymethyl)-2-oxazolidinone
CAS No.:87823-54-9
Molecular Formula:C17H16ClNO4
Molecular Weight:333.771
Hs Code.:
Mol file:87823-54-9.mol

Synonyms:(S)-3-[4-(3-Chloro-benzyloxy)-phenyl]-5-hydroxymethyl-oxazolidin-2-one;(S)-3-{4-[(3-chlorophenyl)methoxy]phenyl}-5-(hydroxymethyl)-2-oxazolidinone;[S(+)] 5-hydroxymethyl 3-p-(meta-chlorobenzyloxy)phenyl oxazolidine-2-one;

Suppliers and Price of (5S)-3-[4-[(3-Chlorophenyl)methoxy]phenyl]-5-(hydroxymethyl)-2-oxazolidinone

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of (5S)-3-[4-[(3-Chlorophenyl)methoxy]phenyl]-5-(hydroxymethyl)-2-oxazolidinone

Chemical Property:

Melting Point:133 °C (ethanol)
PSA：59.00000
LogP:3.30150

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (5S)-3-[4-[(3-Chlorophenyl)methoxy]phenyl]-5-(hydroxymethyl)-2-oxazolidinone

There total 4 articles about (5S)-3-[4-[(3-Chlorophenyl)methoxy]phenyl]-5-(hydroxymethyl)-2-oxazolidinone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 130641-75-7
4-<(3-chlorophenyl)methoxy>nitrobenzene

: 87823-54-9
(S)-3-<4-<(3-chlorophenyl)methoxy>phenyl>-5-(hydroxymethyl)-2-oxazolidinone

Guidance literature:: Multi-step reaction with 3 steps

1: FeCl₃*6H₂O, activated carbon, hydrazine hydrate / CH₂Cl₂ / 30 h

2: 68 percent / ethanol / 1.) 50 deg C, 12 h, 2.) reflux, 12 h

3: 85 percent / sodium methoxide / methanol / 12 h / 105 °C

With sodium methylate; iron(III) chloride; pyrographite; hydrazine hydrate; In methanol; ethanol; dichloromethane;

Reference yield:

: 57181-88-1
4-<(3-chlorophenyl)methoxy>aniline

: 87823-54-9
(S)-3-<4-<(3-chlorophenyl)methoxy>phenyl>-5-(hydroxymethyl)-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / ethanol / 1.) 50 deg C, 12 h, 2.) reflux, 12 h

2: 85 percent / sodium methoxide / methanol / 12 h / 105 °C

With sodium methylate; In methanol; ethanol;

Reference yield:

: 824-78-2
4-nitrophenol sodium salt

: 87823-54-9
(S)-3-<4-<(3-chlorophenyl)methoxy>phenyl>-5-(hydroxymethyl)-2-oxazolidinone

Guidance literature:: Multi-step reaction with 4 steps

1: 82 percent / dimethylformamide / 6 h / 65 °C

2: FeCl₃*6H₂O, activated carbon, hydrazine hydrate / CH₂Cl₂ / 30 h

3: 68 percent / ethanol / 1.) 50 deg C, 12 h, 2.) reflux, 12 h

4: 85 percent / sodium methoxide / methanol / 12 h / 105 °C

With sodium methylate; iron(III) chloride; pyrographite; hydrazine hydrate; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;