HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635569Generated: October 27, 2026
Hydrochloric Acid → 2-Chloro-1-phenylethanol, (+)-
https://huagongshe.com/reaction/635569
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 2-Chloroacetophenone | HCID 10757 | — |
| Reactant | Aluminum isopropoxide | HCID 11143 | — |
| Reactant | Binol | HCID 11762 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Chloro-1-phenylethanol, (+)- | HCID 643323 | — |
Reaction Steps
To a slurry solution of 143 mg (0.5 mmol) of (R)-1,1′-bi-2-naphthol in 10 ml of toluene was added 102 mg (0.5 mmol) of aluminum triisopropoxide at room temperature, and the mixture was stirred at room temperature for 20 minutes and further at 50° C. for 1 hour. Thereto 1.52 ml (20 mmol) of 2-propanol was added and the mixture was stirred further at room temperature for 30 minutes. Thereto 1.55 g (10 mmol) of phenacyl chloride was added and the mixture was further stirred at 50° C. for 4 hours. To the mixture were added 2 ml of 1N hydrochloric acid and 20 ml of water to conduct hydrolysis. The mixture was extracted with ethyl acetate and concentrated to obtain an oily product. The after-treatment and the analysis of the product were then carried out in the same manner as described in Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187966B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-c6efd2ff1c484c3cbab5dbf8a7a0a91c |
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| Source note | uspto-grants-2001_02 |
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