Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091413Generated: October 28, 2026

Water → 2-methyl-1-[3-methyl-5-(tetrahydro-2H-thiopyran-4-yloxy)-1-benzofuran-2-yl]propan-1-ol

https://huagongshe.com/reaction/2091413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant2-methyl-1-[3-methyl-5-(tetrahydro-2H-thiopyran-4-yloxy)-1-benzofuran-2-yl]propan-1-oneHCID 66777811—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-methyl-1-[3-methyl-5-(tetrahydro-2H-thiopyran-4-yloxy)-1-benzofuran-2-yl]propan-1-olHCID 6677832073%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Methyl-1-[3-methyl-5-(tetrahydro-2H-thiopyran-4-yloxy)-1-benzofuran-2-yl]propan-1-one (849 mg) synthesized above was dissolved in methanol (3 mL)-tetrahydrofuran (15 mL), and sodium tetrahydroborate (90%) (202 mg) was added to the solution at 0° C. The reaction mixture was stirred at 0° C. for 30 min. 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. The residue was subjected to silica gel column chromatography (hexane-ethyl acetate 100:0-85:15, v/v) to give the title compound (621 mg, 73%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-e954da755e73445a8379eabc275fd159
Source noteuspto-grants-2013_05