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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390781Generated: October 30, 2026

Trifluoroborane-methyl sulfide → HCID 45483044, compound

https://huagongshe.com/reaction/2390781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroborane-methyl sulfideHCID 11137191—
ReactantHCID 45482661HCID 45482661—
SolventDichloromethaneHCID 6344—
ProductHCID 45483044HCID 45483044—

Reaction Steps

Borontrifluoride-dimethylsulfide (0.13 mL, 1.2 mmol) was dropwise added to a solution of the methoxy compound (52.5 mg, 0.12 mmol) prepared in Example 39 in dichloromethane (4 mL) at room temperature under nitrogen atmosphere, and stirred for 24 hours. The reaction mixture was concentrated by vacuum distillation. The residue was treated in ethyl acetate (100 mL) and brine (50 mL) and the organic layer was dried over anhydrous magnesium sulfate and distilled under vacuum. Purification through column chromatography (silica gel, ethyl acetate) afforded pure hydroxy products (28 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273880B2
Source datasetuspto-grants-2012_09
ORD IDord-0b8f3d380b0b4a9a8caef67e91d0cd30
Source noteuspto-grants-2012_09