HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582925Generated: October 30, 2026
Hydrochloric Acid → 5-Chloro-2,3-dihydro-1H-inden-1-ol
https://huagongshe.com/reaction/582925
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Chloro-1-indanone | HCID 142599 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-2,3-dihydro-1H-inden-1-ol | HCID 22504804 | 83% |
Reaction Steps
A mixture of 2.5 g of 5-chloroindan-1-one and 30 ml of THF is cooled to 0-5° C., 2.5 ml of concentrated NaOH solution and then, in portions, 0.88 g of sodium borohydride are added and the reaction mixture is stirred overnight at RT. It is poured into 100 ml of water, the mixture is acidified to pH 2 by the addition of concentrated HCl solution, extracted with AcOEt, the organic phase is washed with saturated NaCl solution and dried over Na2SO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica using a cyclohexane/AcOEt mixture (80/20; v/v) to give 2.1 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05925768 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-3c979d0db6d44c47a6d47fc5f9d8de67 |
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| Source note | uspto-grants-1999_07 |
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