HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362882Generated: October 30, 2026
Sodium borohydride → HCID 10198426, compound
https://huagongshe.com/reaction/362882
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15896151 | HCID 15896151 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10198426 | HCID 10198426 | 45.4% |
Reaction Steps
A suspension of (E)-2-(4,6-difluoro-3-oxo-1-indanylidene)acetamide (0.100 g, 0.45 mmol) and sodium borohydride (0.017 g, 0.45 mmol) in 95% ethanol was stirred at ambient temperature for 2 hours. The mixture was cooled in an ice bath and quenched with 0.1N hydrochloric acid (3 mL). The ethanol was evaporated in vacuo, and the residue was dissolved in ethyl acetate (50 mL), washed successively with water (2×3 mL) and brine (30 mL), dried over sodium sulfate, filtered, and evaporated in vacuo. The resudue was washed successively with cold ethyl acetate, hexane, and diethyl ether to give 0.046 g (45%) of (E)-2-(4,6difluoro-3-hydroxy-1-indanylidene)acetamide as a white solid; mp 232°-237° C. (dec.) 1H-NMR (DMSO-d6): δ7.06-7.42 (m, 4H), 6.49 (s, 1H), 5.52 (d, 1H), 5.30 (m,1H), 3.44 (m,1H), 3.03 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05872118 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-b521bca281dc433c8faf0047c1c09a90 |
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| Source note | uspto-grants-1999_02 |
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