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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709453Generated: October 27, 2026

Hydrochloric Acid → 2-[2-(4-Fluoro-phenyl)-ethylsulfanyl]-3-(4-hydroxymethyl-phenyl)-propionic acid 2,2,2-trichloro-ethyl ester

https://huagongshe.com/reaction/709453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantBoron trifluorideHCID 6356—
Reactant3-[4-(Tert-butyl-dimethyl-silanyloxymethyl)-phenyl]-2-[2-(4-fluoro-phenyl)-ethylsulfanyl]-propionic acid 2,2,2-trichloro-ethyl esterHCID 131731680—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-[2-(4-Fluoro-phenyl)-ethylsulfanyl]-3-(4-hydroxymethyl-phenyl)-propionic acid 2,2,2-trichloro-ethyl esterHCID 44185046—

Reaction Steps

To a solution of 3-[4-(tert-butyl-dimethyl-silanyloxymethyl)-phenyl]-2-[2-(4-fluoro-phenyl)-ethylsulfanyl]-propionic acid 2,2,2-trichloro-ethyl ester (5.47 g, 9.43 mmol) in anhydrous acetonitrile (200 mL) was dropwise added BF3×Et2O (1.10 mL, 9.43 mmol) at 0° C. The mixture was stirred for 30 min. 2N aq. HCl (50 mL) and H2O (100 mL) were added and the mixture was extracted with DCM. The combined organic layers were dried (MgSO4) and evaporated to give the crude product which was purified by flash chromatography using DCM/MeOH 95:5 as the eluent. The product was obtained as an (3.62 g, 82.5%). 1H NMR (400 MHz, CDCl3): δ 7.19 (d, 2H), 7.10 (d, 2H), 7.01 (m, 2H), 6.87 (t, 2H), 4.65 (d, 1H), 4.56 (m, 3H), 3.48 (dd, 1H), 3.12 (dd, 1H), 2.73-2.91 (m, 5H). Mass Spectrum: M−H+ 464.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181181B2
Source datasetuspto-grants-2015_11
ORD IDord-cb6c7dab94044561b11823284c608196
Source noteuspto-grants-2015_11