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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223560Generated: October 26, 2026

Benzyl chloroformate → Benzyl 4-(2-hydroxy-4-methoxybenzoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/223560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactant(2-Hydroxy-4-methoxyphenyl)(piperidin-4-yl)methanoneHCID 13076390—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-(2-hydroxy-4-methoxybenzoyl)piperidine-1-carboxylateHCID 1307639676.5%

Reaction Steps

To a stirred, ice-cooled mixture of 36.1 g of 4-(2-hydroxy-4-methoxybenzoyl)piperidine, 16.3 g of sodium bicarbonate and 350 ml of dichloromethane, was added dropwise 22.9 ml of benzyl chloroformate in dichloromethane. After the addition was complete, the mixture was stirred at ambient temperature for 1.5 hrs, filtered and the filtrate concentrated to an oil. The oil crystallized. The crystals were collected, washed with hexane and dried to yield 42.4 g (76.5%) of product. Recrystallization from isopropanol gave the analytical sample, mp, 89°-91°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355037
Source datasetuspto-grants-1982_10
ORD IDord-0ae2e7daf56342efac918d9c44a6c397
Source noteuspto-grants-1982_10