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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119404Generated: October 30, 2026

2-Chloro-1,3-benzoxazol-6-yl acetate → benzyl (2S)-1-[6-(acetyloxy)-1,3-benzoxazol-2-yl]-2-piperidinecarboxylate

https://huagongshe.com/reaction/2119404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,3-benzoxazol-6-yl acetateHCID 18340179—
Reactant(2S)-2-((benzyloxy)carbonyl]piperidinium chlorideHCID 86591486—
Productbenzyl (2S)-1-[6-(acetyloxy)-1,3-benzoxazol-2-yl]-2-piperidinecarboxylateHCID 54058787—

Reaction Steps

The title compound was prepared by a similar method to Preparation 2 from (2S)-2-[(benzyloxy)carbonyl]piperidinium chloride [see EP 530167 A1 930303] and 2-chloro-1,3-benzoxazol-6-yl acetate [see Preparation 35]. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 80:10 changing to 40:10, by volume, hexane:ethyl acetate to afford benzyl (2S)-1-[6-(acetyloxy)-1,3-benzoxazol-2-yl]-2-piperidinecarboxylate as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686357B1
Source datasetuspto-grants-2004_02
ORD IDord-e796f463481e4c93ada8d6a43559a51f
Source noteuspto-grants-2004_02