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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044153Generated: October 30, 2026

3-Phenylthiopropan-2-one → 1-(Phenylthio)-2-propanol

https://huagongshe.com/reaction/2044153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenylthiopropan-2-oneHCID 247129—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-(Phenylthio)-2-propanolHCID 9978852%

Reaction Steps

732 mg (19.2 mmol) of NaBH4 were added in portions, while cooling (ice bath), to a solution of 2.46 g (14.8 mmol) of 1-(phenylthio)propan-2-one in methanol (18 ml). Stirring was then carried out for a further 2 h while cooling (ice bath). The mixture was then quenched with AcOH (17 ml) and then concentrated in vacuo. The residue was taken up in an ether/water mixture and neutralized with NaHCO3. The phases were separated and the organic phase was dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by means of CC (EA/hex 15:85), yielding 1.3 g (7.7 mmol, 52%) of 1-(phenylthio)propan-2-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586755B2
Source datasetuspto-grants-2013_11
ORD IDord-cb57b628a4c94485b8184e499b04ed2b
Source noteuspto-grants-2013_11