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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276179Generated: October 26, 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/1276179

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 numberUS06166011
Source datasetuspto-grants-2000_12
ORD IDord-b59b59aa38b344d4a9720646bf126fdc
Source noteuspto-grants-2000_12