Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412656Generated: October 24, 2026

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

https://huagongshe.com/en/reaction/412656

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 minutes. 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 numberUS06562964B1
Source datasetuspto-grants-2003_05
ORD IDord-d28894faf6d1432a999cc21be042e341
Source noteuspto-grants-2003_05