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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446824Generated: November 1, 2026

Triethylamine → 2-Amino-3-(4-fluorobenzoyl)-alpha-(n-propylthio)-phenylacetamide

https://huagongshe.com/reaction/1446824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTert-Butyl hypochloriteHCID 521297—
Reactant2-Amino-4'-fluorobenzophenoneHCID 9837287—
ReactantPentanethioamideHCID 12534254—
SolventDichloromethaneHCID 6344—
Product2-Amino-3-(4-fluorobenzoyl)-alpha-(n-propylthio)-phenylacetamideHCID 1534360656.3%

Reaction Steps

A solution of 21.5 g (0.1 mole) of 4'-fluoro-2-aminobenzophenone in 400 ml of methylene chloride was cooled to -70° C. and 11.5 g (0.1 mole) of 95% t-butylhypochlorite was added over a period of 15 min, keeping the temperature below -66° C. To this solution was added a solution of 13.3 g of 2-n-propylthioacetamide in 50 ml of methylene chloride over a 10 min period. The solution was stirred for 1 hr at -65° to -70° C. and then allowed to warm to 0° C. at which point 10.2 g (0.1 mole) of triethylamine was added. The solution was stirred for 10 minutes and then washed with water. The organic solution was dried over magnesium sulfate. After concentrating under reduced pressure, the residue was crystallized from isopropyl alcohol and dried to give 19.5 g (56%) of yellow crystals melting at 140°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04313949
Source datasetuspto-grants-1982_02
ORD IDord-f0e076c9d25e48799804874a7f19c261
Source noteuspto-grants-1982_02