Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxy-1-indanone | HCID 590547 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-Hydroxyindan | HCID 74233 | 92.9% |
Reaction Steps
A mixture of 4-hydroxy-indan-1-one (5.0 g, 33.7 mmol), sodium cyanoborohydride (6.4 g, 101.1 mmol), and zinc iodide (32.3 g, 101.1 mmol) in dichloroethane, was heated at reflux for two hours. The reaction mixture was then filtered through 50 g SiO2 while still warm, eluting further with dichloroethane. The filtrate was collected and concentrated under vacuum. The residue was added to diethyl ether and the resulting white precipitate was filtered off. The filtrate was collected and concentrated in vacuo to give 4.2 g of the title compound with purity high enough for subsequent use. 400 MHz 1H NMR (DMSO-d6) δ 9.06 (s, 1H), 6.86 (t, 1H, J=7.8 Hz), 6.59 (d, 1H, J=7.8 Hz), 6.48 (d, 1H, J=7.8 Hz), 2.75 (t, 2H, J=7.3 Hz), 2.67 (t, 2H, J=7.3 Hz), 1.92 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06833380B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-597a315ad7274ea8ae5ccb1ef9900ada |
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| Source note | uspto-grants-2004_12 |
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