HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209546Generated: October 31, 2026
Borane;tetrahydrofuran → HCID 57285352, compound
https://huagongshe.com/reaction/2209546
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 57151048 | HCID 57151048 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57285352 | HCID 57285352 | 82% |
Reaction Steps
To a stirred solution of 1.47 g of the (2S)-2-(t-butylthio)propanoic acid in 22 mL of THF at 0° C. was added dropwise 22 mL of 1M borane/THF over a period of 15 min. Stirring was continued at room temperature for 3 h. The reaction was quenched by dropwise addition of cold water. The mixture was extracted with ether. The organic layer was washed with saturated NaHCO3, saturated NaCl solution and dried over Na2SO4. The solvent was evaporated under vacuum and the residue was purified by flash chromatography (10% EtOAc in hexane) to give 1.10 g of (2S)-2-(tert-butylthio)-1-propanol as an oil at 82% yield. Characteristic analytical data are as follows: 1H NMR (300 MHz, CDCl3) δ3.61 (ddd, J=5, 9, 11 Hz, 1H), 3.33 (ddd, J=4, 8, 11 Hz, 1H), 2.89 (m, 1H), 2.31 (dd, J= 4, 9 Hz, 1H, OH), 1.36 (s, 9H), 1.30 (d, J=7 Hz, 3H); [α]D25 -10.3° (c=2.04, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455262 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-1ed0579a0b644e5db8db966d30cf488b |
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| Source note | uspto-grants-1995_10 |
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