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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457210Generated: November 1, 2026

Hydrochloric Acid → 2,2-Difluoro-2-phenylethylamine

https://huagongshe.com/reaction/1457210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant2,2-Difluoro-2-phenylacetamideHCID 269656—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
SolventTetrahydrofuranHCID 8028—
Product2,2-Difluoro-2-phenylethylamineHCID 1263552939%

Reaction Steps

Borane·dimethylsulfide (1.5 ml; 15.4 mmol) was added dropwise over 30 minutes to a solution of the title compound of Step (B) (1 g; 5.84 mmol) in 6 ml of THF at room temperature. After stirring 18 hr at room temperature and 2 hr at reflux, the reaction mixture was cooled to 0° C. and 3 ml of methanol were added carefully over 15 minutes. The solution was saturated with HCl (g) and the cloudy mixture was stirred 6 hr at room temperature, 30 minutes at reflux and 60 hr at room temperature. After removing the volatiles in vacuo, the residue was partitioned between ether (50 ml) and 1N HCl (30 ml). The ether layer was extracted with 1N HCl (10 ml) and the combined aqueous was backwashed with ether (50 ml). After adjusting the pH to 8 with solid NaHCO3, 1N NaOH (1 ml) was added and the aqueous layer was extracted with ether (50 ml). After washing with saturated NaHCO3 solution (25 ml), water (25 ml) and brine (25 ml), the ether layer was dried (MgSO4) and concentrated to afford 355 mg (39%) of the title compound of this step as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846990
Source datasetuspto-grants-1998_12
ORD IDord-b4e7d949ea99474e85feca60b639b0b4
Source noteuspto-grants-1998_12