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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412664Generated: October 30, 2026

Ethyl Acetate → ethyl (2S)-1-(1,3-benzothiazol-2-yl)-2-piperidinecarboxylate

https://huagongshe.com/reaction/412664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTriethylamine hydrochlorideHCID 11130—
Reactant2-ChlorobenzothiazoleHCID 11987—
ReactantEthyl (2S)-2-piperidinecarboxylateHCID 736055—
CatalystCopperHCID 23978—
SolventO-XyleneHCID 7237—
Productethyl (2S)-1-(1,3-benzothiazol-2-yl)-2-piperidinecarboxylateHCID 5701620581.9%

Reaction Steps

2-Chloro-1,3-benzothiazole (503 mg) was added to a suspension of ethyl (2S)-2-piperidinecarboxylate (471 mg) [J.A.C.S. (1993), 115(22), 9925-9938], triethylamine hydrochloride (414 mg) and copper powder (38 mg) in xylene (5 ml). The reaction mixture was refluxed for 28 hours, after which time ethyl acetate (20 ml) was added to the cooled mixture and the solids filtered off. The organic layer was washed with water, dried over magnesium sulphate and the solvent removed under reduced pressure to afford ethyl (2S)-1-(1,3-benzothiazol-2-yl)-2-piperidinecarboxylate (705 mg) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562964B1
Source datasetuspto-grants-2003_05
ORD IDord-dc04ecab06f84771aa20652422f9cdc2
Source noteuspto-grants-2003_05