HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978117Generated: October 30, 2026
Sodium borohydride → HCID 13849495, compound
https://huagongshe.com/reaction/978117
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13849489 | HCID 13849489 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13849495 | HCID 13849495 | — |
Reaction Steps
To a mixture of ethyl-3-methyl-4-(2-oxopropoxy)benzofuran-2-carboxylate (1.9 g, 6.8 mmoles, Example 117) in ethanol (100 ml) at 5° C. was added in portions, sodium borohydride (254 mg, 6.8 mmoles). The mixture was stirred for 10 minutes at 5° C. and 30 minutes at room temperature. The reaction was quenched with saturated ammonium chloride solution (1.5 ml) and concentrated. The residue was taken up in ether (100 ml), washed with water (25 ml), dried with Na2SO4, filtered and concentrated to obtain the title compound as an oil which crystallized on standing. The crystals were stirred with 25% ether in hexane (50 ml) for 30 minutes, filtered and then air dried, m.p. 94°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663347 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-8ec02821d77d4bbd9a84638053fa146d |
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| Source note | uspto-grants-1987_05 |
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