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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852433Generated: November 1, 2026

Water → HCID 86729351, compound

https://huagongshe.com/reaction/1852433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantBromodifluoromethyl diethylphosphonateHCID 144101—
ReactantHCID 53405056HCID 53405056—
SolventAcetonitrileHCID 6342—
ProductHCID 86729351HCID 86729351—

Reaction Steps

(5-Bromo-2-sulfanylphenyl)methanol (0.50 g, 2.8 mmol) was dissolved in MeCN (11.4 mL) followed by the addition of water (11.4 mL) and solid potassium hydroxide (2.56 g, 45.6 mmol). The mixture was plunged into a −78° C. bath and when the mixture began to freeze diethyl[bromo(difluoro)methyl]phosphonate (1.22 g, 4.56 mmol) was added all at once and the cold bath was removed. The mixture was allowed to warm to ambient temperature and was stirred for 20 minutes. The mixture was then partitioned between EtOAc and water. The organic layer was washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by MPLC on silica gel (using a gradient elution of 0-25% EtOAc/hexanes). Desired fractions were identified, combined, and concentrated in vacuo to afford the title compound. 1H NMR (500 MHz, CDCl3): δ 7.76 (s, 1H), 7.47 (m, 2H), 6.80 (t, J=56.5 Hz, 1H), 4.87 (s, 2H), 1.96 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962608B2
Source datasetuspto-grants-2015_02
ORD IDord-ec8b35c512af42a7bcb85d922b2c84f9
Source noteuspto-grants-2015_02