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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298862Generated: November 3, 2026

2,4,4,6-Tetrabromocyclohexa-2,5-dienone → methyl (2S)-1-(6-bromo-1,3-benzoxazol-2-yl)-2-piperidinecarboxylate

https://huagongshe.com/reaction/2298862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,4,6-Tetrabromocyclohexa-2,5-dienoneHCID 88433—
Reactantmethyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylateHCID 10220819—
SolventDichloromethaneHCID 6344—
Productmethyl (2S)-1-(6-bromo-1,3-benzoxazol-2-yl)-2-piperidinecarboxylateHCID 994977195.1%

Reaction Steps

2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one (4.7 g) was added to a solution of methyl (2S)-1-(1,3-benzoxazol-2-yl)-2-piperidinecarboxylate (3.0 g) [see Preparation 2] in dichloromethane (60 ml) at −10° C. over a period of 10 mins. The reaction mixture was then warmed to room temperature and diluted with dichloromethane. The organic layer was washed with saturated sodium hydrogen carbonate, then with 1N sodium hydroxide solution, dried over sodium sulphate and the solvent removed under reduced pressure to afford methyl (2S)-1-(6-bromo-1,3-benzoxazol-2-yl)-2-piperidinecarboxylate (3.7 g) as a purple coloured oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495549B1
Source datasetuspto-grants-2002_12
ORD IDord-63d384c824a24caa8759f8f72013b685
Source noteuspto-grants-2002_12