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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807952Generated: October 30, 2026

Borane;tetrahydrofuran → HCID 67178219, compound

https://huagongshe.com/reaction/1807952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant1-(3-Chloro-5-fluorophenyl)ethan-1-oneHCID 2757531—
ReactantCID 53628436HCID 53628436—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67178219HCID 6717821989%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (R)-MeCBS oxazaborolidine (2.9 ml, 1M solution in toluene) in dry tetrahydrofuran (5 ml) was added dropwise borane-THF complex (17.4 ml, 1M solution in tetrahydrofuran) under an argon atmosphere. The solution was cooled to 0° C. and 3′-chloro-5′-fluoroacetophenone (5.0 g) dissolved in dry tetrahydrofuran (5 ml) was added dropwise to the reaction mixture in 40 min. The reaction mixture was stirred for 1 h at 0° C. and was slowly quenched with methanol (5 ml) followed by addition of HCl 4M in ethanol (1 ml). After stirring the mixture for 5 min at 0° C., the cooling bath was removed and the white suspension was stirred at room temperature for 30 min. The suspension was filtered over celite and the filtrate was evaporated over silica gel for purification. Column chromatography (SiO2; heptane/EtOAc) afforded (S)-1-(3-chloro-5-fluoro-phenyl)-ethanol (4.50 g, 89%) as a colourless liquid. 1H NMR (300 MHz, CDCl3, δ): 1.48 (d, J=6.3 Hz, 3H), 1.92 (bs, 1H), 4.87 (q, J=6.6 Hz), 6.98 (m, 2H), 7.16 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357712B2
Source datasetuspto-grants-2013_01
ORD IDord-a12dd66812804bf9b8044bea88acc517
Source noteuspto-grants-2013_01