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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761846Generated: October 28, 2026

3,5-Di-tert-butyl-4-hydroxybenzoyl chloride → HCID 14300313, compound

https://huagongshe.com/reaction/1761846

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Di-tert-butyl-4-hydroxybenzoyl chlorideHCID 3787187—
ReactantBenzyl 1,4-diazepane-1-carboxylateHCID 4384955—
SolventAcetonitrileHCID 6342—
ProductHCID 14300313HCID 14300313—

Reaction Steps

A mixture of 13.4 g (0.05 mol) of 3,5-di-tert.-butyl-4-hydroxybenzoyl chloride and 12.4 g (0.053 mol) of 1-benzyloxycarbonylhomopiperazine in 200 ml of acetonitrile is heated under reflux, with stirring, for 6 hour. The solvent is then removed by distillation under reduced pressure, the residue is partitioned between methylene chloride and dilute hydrochloric acid, and the organic phase is separated off and washed with saturated brine. After drying over sodium sulfate and removal of the solvent by distillation under reduced pressure, the crystalline residue is digested with hot diisopropyl ether, filtered off with suction, washed with diisopropyl ether and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04829061
Source datasetuspto-grants-1989_05
ORD IDord-adf67d0c2e6d4c239ebb395b912a1ae6
Source noteuspto-grants-1989_05