HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047107Generated: November 2, 2026
Sodium borohydride → (1S,3S)-6-chloro-3-phenylindan-1-ol
https://huagongshe.com/reaction/1047107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (S)-6-chloro-3-phenylindan-1-one | HCID 11997855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (1S,3S)-6-chloro-3-phenylindan-1-ol | HCID 11521607 | 90.1% |
Reaction Steps
(S)-6-chloro-3-phenylindan-1-one (IVa) (isolated as in example 7) (23 g) is added in small portions to a suspension of sodium borohydride (1.6 g) in ethanol (160 ml) at 3-5° C. After the addition has been finalised, the mixture is allowed to reach room temperature. The reaction mixture is stirred for 2.75 hours, where after it is evaporated to dryness. The residue is dissolved in a mixture of water (150 ml) and ethyl acetate (200 ml), the phases are separated, and the water phase is extracted with ethyl acetate (100 ml). The organic phases are combined, washed with water (100 ml), dried with magnesium sulphate, filtered and evaporated to dryness. The residue is recrystallised from heptanes (250 ml), giving 20.9 g (90%) of the title product as a solid. Melting point 108.9° C., NMR conforms to structure, [α]D20 +48.30° (c=1.0, methanol). CHN calculated for C15H13OCl: C, 73.62; H, 5.35; found: C, 73.55; H, 5.29. >99% ee according to the chiral analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569499B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-c3c233d5d71745a2ab4bc0e484c2adfe |
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| Source note | uspto-grants-2013_10 |
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