HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842338Generated: October 31, 2026
Hydrochloric Acid → 1-Phenylethanol, (S)-
https://huagongshe.com/reaction/842338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Phenylethanol, (S)- | HCID 443135 | 43% |
Reaction Steps
To the catalyst solution was added a degassed 0.1M solution of KOH in 2-propanol, followed by a solution of acetophenone in 2-propanol. The mixture was warmed to 60° C. and stirred at ambient temperature under nitrogen for 1 h, then worked up by neutralising with dilute hydrochloric acid and concentrating by vacuum distillation. The residue was diluted with ethyl acetate and washed with an equal volume of saturated aqueous sodium chloride. The organic layer was separated, dried over magnesium sulphate, separated from the solid and freed of solvent to give crude (S)-1-phenylethanol (0.9 g). Yield 43%, ee 80%. The turnover number, integrated over 1 h, was 410 h−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06372931B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-4e126b73a0cd4caa845167f08b5bc8b2 |
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| Source note | uspto-grants-2002_04 |
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