HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807952Generated: October 30, 2026
Borane;tetrahydrofuran → HCID 67178219, compound
https://huagongshe.com/reaction/1807952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 1-(3-Chloro-5-fluorophenyl)ethan-1-one | HCID 2757531 | — |
| Reactant | CID 53628436 | HCID 53628436 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67178219 | HCID 67178219 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357712B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-a12dd66812804bf9b8044bea88acc517 |
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| Source note | uspto-grants-2013_01 |
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