HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296041Generated: October 30, 2026
5-Chloro-1-indanone → 5-Chloro-2,3-dihydro-1H-inden-1-ol
https://huagongshe.com/reaction/1296041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Chloro-1-indanone | HCID 142599 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Chloro-2,3-dihydro-1H-inden-1-ol | HCID 22504804 | — |
Reaction Steps
To a precooled (5–10° C.) solution of 5-chloro-indan-1-one (2.0 g, 12 mmoles) in 33 mL of anhydrous methanol was added sodium borohydride (0.43 g, 11 mmoles). The reaction mixture was stirred at 10° C. for 2 hrs and then at room temperature for 18 hrs. The reaction mixture was evaporated to afford a yellow residue. The residue was dissolved in 200 mL of diethyl ether and then washed with water (2×100 mL), with 0.10 N hydrochloric acid (2×100 mL), and then with brine (100 mL). The organic layer was separated, dried (sodium sulfate), filtered, and the filtrate was evaporated to provide the title compound in good purity. MS m/z 167 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244763B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-6f126b94db9f44529457729dac328bc6 |
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| Source note | uspto-grants-2007_07 |
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