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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970107Generated: October 31, 2026

Dimethylformamide → 2-(4-Chlorophenoxy)benzeneacetyl chloride

https://huagongshe.com/reaction/1970107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(2-(4-Chlorophenoxy)phenyl)acetic acidHCID 12245871—
SolventTolueneHCID 1140—
Product2-(4-Chlorophenoxy)benzeneacetyl chlorideHCID 23148661—

Reaction Steps

[2-(4-chloro-phenoxy)-phenyl]-acetic acid (IX) (47.3 grams; 180 mmol) was suspended in toluene (140 ml) at 48° C. To this suspension dimethyl-formamide (4.0 ml) and SOCl2 (19.8 ml; 271 mmol; 1.5 eq) in toluene (18 ml) were added. After 10 min the reaction mixture was concentrated under vacuo and stripped twice with toluene, to yield a brownish oil of [2-(4-chloro-phenoxy)-phenyl]-acetyl chloride. The oil was suspended in toluene (75 ml). To the suspension was added at 5° C. a solution of sarcosine methylester (30.3 grams 217 mmol) and triethylamine (57 ml) in a mixture of dimethyl-formamide (236 ml) and toluene (47 ml). The brownish suspension was stirred for 2 hours at room temperature. To the reaction mixture water (750 ml) was added and the mixture was extracted twice with ethyl acetate (500 ml). The organic phase was washed with saturated brine (700 ml) and dried on magnesium sulphate. The solvent was removed in vacuum to yield methyl-N-[2-(4-chloro-2-phenoxyphenyl)-1-oxethyl]-N-methylglycinate (X) (61.3 grams, 202 mmol) as a brownish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426610B2
Source datasetuspto-grants-2013_04
ORD IDord-d336932884524a45837b8ec9d4ba540c
Source noteuspto-grants-2013_04