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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380252Generated: November 1, 2026

Methanol → HCID 23326057, compound

https://huagongshe.com/reaction/1380252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23326074HCID 23326074—
SolventWaterHCID 962—
ProductHCID 23326057HCID 2332605794.5%

Reaction Steps

To a stirred solution of 140.5 parts of 4-[bis(4-fluorophenyl)hydroxymethyl]-1-(phenylmethyl)pyridinium bromide in 640 parts of methanol were added portionwise, during a 2 hours-period, 15.1 parts of sodium borohydride at room temperature (cooling in ice-water was necessary). Upon completion, the whole was stirred and refluxed for 30 minutes. After cooling to room temperature, 800 parts of water were added. The whole was allowed to stand overnight. The reaction mixture was evaporated till all traces of methanol were removed. 1040 Parts of dichloromethane were added. The layers were separated. The organic layer was washed with 200 parts of water, dried, filtered and evaporated. The residue was taken up in dry methylbenzene and the whole was evaporated, yielding 111 parts (94.5%) of α,α-bis(4-fluorophenyl)-1,2,3,6-tetrahydro-1-(phenylmethyl)-4-pyridinemethanol as an oily residue (intermediate 28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581171
Source datasetuspto-grants-1986_04
ORD IDord-cb1dbdd84f6c4048b0343bb054a473b2
Source noteuspto-grants-1986_04