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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978117Generated: October 30, 2026

Sodium borohydride → HCID 13849495, compound

https://huagongshe.com/reaction/978117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13849489HCID 13849489—
SolventEthanolHCID 702—
ProductHCID 13849495HCID 13849495—

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663347
Source datasetuspto-grants-1987_05
ORD IDord-8ec02821d77d4bbd9a84638053fa146d
Source noteuspto-grants-1987_05