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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259721Generated: October 28, 2026

Triethylamine → 2-Amino-3-benzoyl-5-chloro-α-(methylthio)benzeneacetamide

https://huagongshe.com/reaction/2259721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
ReactantTert-Butyl hypochloriteHCID 521297—
Reactant2-(Methylthio)acetamideHCID 547873—
SolventDichloromethaneHCID 6344—
Product2-Amino-3-benzoyl-5-chloro-α-(methylthio)benzeneacetamideHCID 67079956—

Reaction Steps

To a cold (-70° C.) solution of 12.77 g (0.055 mole) of 2-amino-5-chlorobenzophenone in 300 mL of methylene chloride, under nitrogen atmosphere, was added 6.0 g (0.552 mole) of t-butylhypochlorite in 20 mL of methylene chloride. After the reaction was stirred for an additional 15 min, a suspension of 5.8 g (0.055 mole) of α-(methylthio)acetamide in 150 mL of methylene chloride was added. The mixture was stirred at -65° C. for 1 h. Triethylamine (5.6 g, 0.055 mole) was added and the solution was allowed to warm to room temperature. The reaction mixture was extracted with water and the organic layer dried over magnesium sulfate. The volume of the solution was reduced in vacuo to about 200 mL and the product crystallized as a yellow solid, m.p. 173.5°-174.5° C. Yield was 6.86 g (37.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475034
Source datasetuspto-grants-1995_12
ORD IDord-a425f2e364eb4008be119daaabf0d083
Source noteuspto-grants-1995_12