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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374819Generated: October 30, 2026

Water → HCID 15294977, compound

https://huagongshe.com/reaction/374819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19002779HCID 19002779—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 15294977HCID 1529497763.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

50 mg of (6-methoxy-2-(4-oxocyclohexyl)benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]phenyl]methanone is dissolved in 4 mL of methanol and 0.5 mL of THF and cooled with ice. 6 mg of sodium borohydride is added, and this mixture is agitated at 0° C. for 15 minutes. Water is added to the reaction mixture, and the organic layer is extracted with ethyl acetate, then washed with water and dried with anhydrous sodium sulfate, after which the solvent is distilled off. The crude product thus obtained is refined by TLC (developing solvent was chloroform:methanol=19:1), which gives 32 mg of [6-methoxy-2-(4-hydroxycyclohexyl)benzo[b]thien-3-yl)[4-[2-(1-piperidinyl)ethoxy]phenyl]methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482950
Source datasetuspto-grants-1996_01
ORD IDord-ec05ef71272d4df6acd1d7e1eadbd3e0
Source noteuspto-grants-1996_01