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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378862Generated: November 3, 2026

Chloroform → N-(4-iso-propylbenzenesulfonyl)-alpha-(4-bromomethyl-2-n-propylphenoxy)-3,4-methylenedioxyphenylacetamide

https://huagongshe.com/reaction/1378862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantAmmonium HydroxideHCID 14923—
ReactantPhosphorus tribromideHCID 24614—
ReactantN-(4-iso-propylbenzenesulfonyl)-alpha-(2-n-propyl-4-hydroxymethylphenoxy)-3,4-methylenedioxyphenylacetamideHCID 19080378—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductN-(4-iso-propylbenzenesulfonyl)-alpha-(4-bromomethyl-2-n-propylphenoxy)-3,4-methylenedioxyphenylacetamideHCID 22912502—

Reaction Steps

To a solution of 0.200 g (0.381 mmol) of the product of Example 65 dissolved in 1.5 mL of diethyl ether was added 0.837 mL (0.837 mmole) of 1.0M phosphorus tribromide in methylene chloride solution under nitrogen at 0° C. The reaction mixture was stirred at 0° C. for 2 hours when TLC analysis (80:15:1 CHCl3 --MeOH--NH4OH) indicated that the reaction was nearly complete. The reaction was quenched at 0° C. with water and then partitioned with EtOAc. The aqueous portion was separated and the EtOAc portion was washed with brine (2×10 mL). The EtOAc portion was then dried over MgSO4, filtered, evaporated to a residue, and then used in the next step of the reaction scheme.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668176
Source datasetuspto-grants-1997_09
ORD IDord-2164ac6a416d47baae2666c78468c05b
Source noteuspto-grants-1997_09