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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484713Generated: October 28, 2026

4-Bromoanisole → HCID 23326077, compound

https://huagongshe.com/reaction/484713

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
ReactantTetrahydrofuranHCID 8028—
ReactantMagnesiumHCID 5462224—
ReactantHCID 23326081HCID 23326081—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
ProductHCID 23326077HCID 23326077—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a stirred and refluxing Grignard complex previously prepared starting from 112.2 parts of 1-bromo-4-methoxybenzene, 15 parts of magnesium and 540 parts of tetrahydrofuran was added dropwise a solution of 84 parts of ethyl 4-(4-fluorobenzoyl)-1-piperidinecarboxylate in 360 parts of tetrahydrofuran. Upon completion, stirring was continued for 2 hours at reflux. After cooling to 10° C., the reaction mixture was poured onto a mixture of 300 parts of crushed ice and 40 parts of acetic acid. The whole was stirred for 5 minutes. 360 Parts of methylbenzene were added. The organic layer was separated, dried, filtered and evaporated, yielding 100 parts of ethyl 4-[(4-fluorophenyl)hydroxy(4-methoxyphenyl)-methyl]-1-piperidinecarboxylate as an oily residue (intermediate 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04533665
Source datasetuspto-grants-1985_08
ORD IDord-263bd7bfb587402a98ee2e1c73ba261a
Source noteuspto-grants-1985_08