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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531434Generated: October 31, 2026

Sodium borohydride → HCID 12016896, compound

https://huagongshe.com/reaction/1531434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 11845284HCID 11845284—
SolventIsopropanolHCID 3776—
SolventChloroformHCID 6212—
ProductHCID 12016896HCID 12016896—

Reaction Steps

8-Fluoro-3-nitro-2H-1-benzopyran-5-carboxamide (730 mg, 3.1 mmol) was slurried in chloroform (75 mL) and isopropyl alcohol (25 mL). To the stirred mixture, silica gel (2.2 g, 230-400 mesh ASTM) was added followed by powdered sodium borohydride (255 mg, 6.2 mmol) portionwise over a period of 15 min. After the addition was complete, the reaction was stirred for 20 min. and the reaction was then quenched by the addition of acetic acid (2 mL) and stirred for an additional 30 min. The insoluble material was filtered off and the solvent removed in vacuo. The residue was partitioned between ethyl acetate and water. The aqueous phase was extracted with ethyl acetate, the combined ethyl acetate phases were treated with brine, dried with MgSO4, filtered, and the solvent was removed in vacuo to give 0.67 g (91% yield) of an off-white solid as the title compound (mp 191.0-191.5° C.). EIMS (70 eV) m/z (relative intensity) 240 (1, M+), 195 (17), 194 (100), 193 (17), 177 (26), 151 (44), 149 (27), 148 (18), 123 (23), 103 (48), 102 (11), 101 (29), 96 (13), 95 (15), 94 (11), 88 (41), 83 (14), 77 (25), 76 (11), 75 (39), 74(23), 70 (10), 63 (11), 60 (11), 51 (17), 50 (10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197978B1
Source datasetuspto-grants-2001_03
ORD IDord-01fb2c84f3f54e7bbe57dd056185a1bf
Source noteuspto-grants-2001_03