Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354392Generated: November 2, 2026

Water → 2-[[(1S)-2-Amino-1-phenylethyl]oxy]-4-chloro-5-fluorobenzonitrile (E)-butenedioate

https://huagongshe.com/reaction/1354392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylphosphineHCID 11776—
ReactantFumaric AcidHCID 444972—
Reactant2-[[(1S)-2-Azido-1-phenylethyl]oxy]-4-chloro-5-fluorobenzonitrileHCID 86598974—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-[[(1S)-2-Amino-1-phenylethyl]oxy]-4-chloro-5-fluorobenzonitrile (E)-butenedioateHCID 131726460—

Reaction Conditions

Temperature60 °C

Reaction Steps

The product from step (b) (2.79 g) in dry THF (80 ml) was treated with triphenylphosphine (3.47 g) and water (12 ml) and the mixture heated at 60° C. for 2 h. The reaction mixture was cooled, poured into water, and extracted with ethyl acetate which was washed with water and dried (MgSO4). The solvent was evaporated and the residue purified by chromatography (silica, ethyl acetate and then 10% 7M ammonia in methanol/dichloromethane as eluent) to give an oil. This was dissolved in ethanol (10 ml), treated with fumaric acid (70.3 mg) and heated until a clear solution was obtained. The mixture was evaporated and the residue triturated with ether to give after filtration and drying in vacuo the final compound (222 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223794B2
Source datasetuspto-grants-2007_05
ORD IDord-b319908457fb432397bcdd58aba72b35
Source noteuspto-grants-2007_05