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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283622Generated: October 25, 2026

Triethylamine → 7-(4-Chlorobenzoyl)-3-methylthioindolin-2-one

https://huagongshe.com/reaction/1283622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-4'-chlorobenzophenoneHCID 76166—
ReactantEthyl (methylthio)acetateHCID 78199—
ReactantTert-Butyl hypochloriteHCID 521297—
SolventDichloromethaneHCID 6344—
Product7-(4-Chlorobenzoyl)-3-methylthioindolin-2-oneHCID 1292354933%

Reaction Conditions

Temperature-65 °C

Reaction Steps

A solution of 23.1 g. (0.1 mole) of 2-amino-4'-chlorobenzophenone in 400 ml. of methylene chloride was cooled to -65°C. and treated dropwise with 12.4 g. (0.1 mole) of t-butyl hypochlorite. After 15 min., 13.4 g. of ethyl α-(methylthio)acetate (0.1 mole) was added dropwise maintaining -65°C. temperature. After 11/2 hr. 10.1 g. of triethylamine (0.1 mole) was added and the reaction mixture allowed to come to room temperature. The solution was then washed with water and stripped. The residue was taken into methanol and brought to reflux at which time lN hydrochloric acid was added and the resulting mixture refluxed overnight. The mixture was cooled, resulting precipitate filtered off and recrystallized from toluene, giving 10 g. of a cream colored solid. The product (33% yield) melted at 186°-188°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975531
Source datasetuspto-grants-1976_08
ORD IDord-76ff40f27ddd4b5e9334ff41f552e477
Source noteuspto-grants-1976_08