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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390777Generated: October 29, 2026

Trifluoroborane-methyl sulfide → HCID 45483006, compound

https://huagongshe.com/reaction/2390777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroborane-methyl sulfideHCID 11137191—
ReactantHCID 45483042HCID 45483042—
SolventDichloromethaneHCID 6344—
ProductHCID 45483006HCID 45483006—

Reaction Steps

Borontrifluoride-dimethylsulfide (0.13 mL, 1.2 mmol) was dropwise added to a solution of the methoxy compound (45.7 mg, 0.12 mmol) prepared in Example 34 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 (24 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273880B2
Source datasetuspto-grants-2012_09
ORD IDord-edb5c7e800224119b40aa3a84246ede8
Source noteuspto-grants-2012_09