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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651477Generated: November 3, 2026

Chloroacetyl chloride → 5-t-butyl-2-methoxy-3-(chloroacetamido) phenyl N-t-butylsulfonamide

https://huagongshe.com/reaction/1651477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-t-butyl-2-methoxy-3-aminophenyl N-t-butyl sulfonamideHCID 15029586—
SolventDichloromethaneHCID 6344—
Product5-t-butyl-2-methoxy-3-(chloroacetamido) phenyl N-t-butylsulfonamideHCID 15029587—

Reaction Steps

A solution of chloroacetyl chloride (4.4 ml) in dichloromethane (40 ml) was added dropwise to a cooled and stirred solution of 5-t-butyl-2-methoxy-3-aminophenyl N-t-butyl-sulfonamide (15.6 g) and diisopropylethylamine (9.5 ml) in dichloromethane (100 ml). The solution was left standing at ambient temperature for 2 hours and then washed with a 2% solution of citric acid. The organic phase was dried and evaporated. Recrytallization from aqueous ethanol gave the title compound (16.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929269
Source datasetuspto-grants-1990_05
ORD IDord-979e8240d54b4415a395bd82d5be5d51
Source noteuspto-grants-1990_05