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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091419Generated: November 2, 2026

Water → HCID 66777218, compound

https://huagongshe.com/reaction/2091419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66777063HCID 66777063—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66777218HCID 6677721890%

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyclohexyl[3-methyl-5-(tetrahydrofuran-2-ylmethoxy)-1-benzofuran-2-yl]methanone (260 mg) synthesized above was dissolved in methanol (0.5 mL)-tetrahydrofuran (2.5 mL), and sodium tetrahydroborate (90%) (64 mg) was added to the solution at 0° C. The reaction mixture was stirred at 0° C. for 2.5 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated to give the title compound (235 mg, 90%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-f345990e52244cdb8ffd9b845e87242a
Source noteuspto-grants-2013_05