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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209546Generated: October 31, 2026

Borane;tetrahydrofuran → HCID 57285352, compound

https://huagongshe.com/reaction/2209546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantHCID 57151048HCID 57151048—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57285352HCID 5728535282%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455262
Source datasetuspto-grants-1995_10
ORD IDord-1ed0579a0b644e5db8db966d30cf488b
Source noteuspto-grants-1995_10