HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679082Generated: October 30, 2026
1,3-Indandione → 3-Hydroxy-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/reaction/1679082
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Indandione | HCID 11815 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 3-Hydroxy-2,3-dihydro-1H-inden-1-one | HCID 176448 | 95% |
Reaction Steps
A mixture of 73.25 g. (0.5 mole) of 1,3-indandione, 10.0 g. of 10% Pd on charcoal and 800 ml. of 2B-ethanol was added on the 1 liter flask of a Brown Hydrogenator, and hydrogen equivalent to 125 ml. of 1M sodium borohydride solution was added at room temperature and atmospheric pressure (0.5 mole H2). The solution was filtered through a bed of Celite Filter Aid, and the bed washed with ethanol. The ethanol solution was concentrated, and from the concentrate, a small amount of white solid separated, 1,3-indanediol, 1,6 g., m.p. 182°-187°. This by-product was filtered off and discarded. Evaporation of the filtrate gave 70.2 g. of nearly colorless oil (yield > 95%) which can be used directly in the aldehyde condensation. The IR spectrum of the product showed typical hydroxyl and carbonyl absorption.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04078934 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-00dd33ff56c341d5a76ca08145ac81ca |
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| Source note | uspto-grants-1978_03 |
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