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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378338Generated: November 1, 2026

4-Chlorobutyryl chloride → Methyl 4-(4-chloro-1-oxobutyl)-alpha,alpha-dimethylbenzeneacetate

https://huagongshe.com/reaction/2378338

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobutyryl chlorideHCID 78370—
ReactantMethyl 2-methyl-2-phenylpropanoateHCID 143498—
ReactantAluminum(III) ChlorideHCID 6451240—
ProductMethyl 4-(4-chloro-1-oxobutyl)-alpha,alpha-dimethylbenzeneacetateHCID 10062338110.9%

Reaction Conditions

Temperature-10 °C

Reaction Steps

MDC (600 ml) and aluminum chloride (347 gms) were charged to a reactor and chilled to −10° C. Methyl-2-methyl-2 phenyl-propanoate (Intermediate 4) (500 gms) was dissolved in MDC (650 ml) and added slowly through a dropper at −10 to 0° C. to obtain mixture A. MDC (600 ml) and aluminum chloride (520 gms) were charged to a different reactor, and chilled to −10° C. 4-chloro butyryl chloride (550 gms) was dissolved in MDC (650 ml) and added slowly through a dropper at −10 to 0° C. to obtain mixture B. Both mixtures A and B were stirred for 45 minutes at −10 to 0° C. separately. Mixture A was added to mixture B slowly at −10 to 0° C. and the reaction monitored by GC for completion (24 hours). The mass was quenched slowly in conc. HCl (1 ltr) at 10-20° C. and stirred for 30 minutes. The MDC layer was separated and the aqueous layer extracted with MDC (500 ml). The combined MDC layer was dried over sodium sulfate and concentrated under vacuum to obtain 880 gms of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470789B2
Source datasetuspto-grants-2008_12
ORD IDord-938661fdc30b478f959ca4a587da5a87
Source noteuspto-grants-2008_12