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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446820Generated: October 31, 2026

Triethylamine → HCID 20552957, compound

https://huagongshe.com/reaction/1446820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
Reactant2-[(4-chlorophenyl)sulfanyl]acetamideHCID 242267—
ReactantTert-Butyl hypochloriteHCID 521297—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20552957HCID 20552957—

Reaction Steps

To a cold (-70° C.) solution of 20 g (0.0863 mole) of 2-amino-5-chlorobenzophenone in 500 ml of methylene chloride under nitrogen atmosphere was added a solution of 9.48 g (0.088 mole) of t-butyl hypochlorite in 50 ml of methylene chloride. After an additional 15 min stirring, a solution of 17.35 g (0.0863 mole) of α-(4-chlorophenylthio)acetamide in 500 ml of a 50/50 mixture of tetrahydrofuran and methylene chloride was added. The mixture was stirred at -70° C. for 2 hr, 8.72 g (0.0863 mole) of triethylamine was added, and the stirred solution was allowed to warm to room temperature over a period of 2 hr. The reaction mixture was extracted with several portions of water and the organic layer dried over magensium sulfate. The volume of liquid was reduced to about 500 ml. Methylene chloride, 500 ml, was added to precipitate the product which after filtration and drying weighed 16.62 g (44.7%). The yellow solid melted at 198°-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04313949
Source datasetuspto-grants-1982_02
ORD IDord-4983969e331c4cf0891e622fe0528b16
Source noteuspto-grants-1982_02