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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901049Generated: October 29, 2026

Diisopropylamine → HCID 23370104, compound

https://huagongshe.com/reaction/1901049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPhenyl chloroformateHCID 15891—
ReactantN-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamideHCID 23370116—
SolventDichloromethaneHCID 6344—
ProductHCID 23370104HCID 233701041,095.8%

Reaction Steps

N-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamide (0.85 g) and diisopropylamine (0.39 ml) were suspended in dichloromethane (20 ml) and a solution of phenyl chloroformate (16.8 g) in dichloromethane (30 ml) was added dropwise under ice-cooling. After stirring the mixture overnight, the reaction solution was washed with water, saturated saline, dried over anhydrous MgSO4 and the solvent was distilled off. Purification of the residue by a silica gel column chromatography (chloroform:ethyl acetate=10:1) followed by crystallization from hexane/ethyl acetate afforded phenyl N-[2-(3,5-di-t-butyl-4-hydroxybenzoylamino)phenyl]carbamate (12.6 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576335
Source datasetuspto-grants-1996_11
ORD IDord-4e8c09844fd24b25af4c01a57dab1cc3
Source noteuspto-grants-1996_11