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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390775Generated: October 30, 2026

Trifluoroborane-methyl sulfide → HCID 45482646, compound

https://huagongshe.com/reaction/2390775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroborane-methyl sulfideHCID 11137191—
ReactantHCID 45483002HCID 45483002—
SolventDichloromethaneHCID 6344—
ProductHCID 45482646HCID 45482646—

Reaction Steps

Borontrifluoride-dimethylsulfide (0.13 mL, 1.2 mmol) was dropwise added to a solution of the methoxy compound (45.6 mg, 0.12 mmol) prepared in Example 23 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 (31 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273880B2
Source datasetuspto-grants-2012_09
ORD IDord-44c7da1dccf646d694f501f54297d19e
Source noteuspto-grants-2012_09