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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474343Generated: November 2, 2026

Sodium borohydride → HCID 66643999, compound

https://huagongshe.com/reaction/1474343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 77231251HCID 77231251—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 66643999HCID 66643999—

Reaction Steps

To a flask charged with methyl 4-allyl-2-formyl-6-methoxybenzoate (0.77 g, 1 mmol) was added sodium borohydride (0.36 g, 9.33 mmol); the mixture was then dissolved in MeOH (10 mL) and stirred for 18 h at room temp. LC indicated completion of the reaction. The mixture was diluted with EtOAc (150 mL) and washed with brine (2×100 mL). The organic layer was then separated, dried(Na2SO4), filtered and concentrated in vacuo. The resulting residue was purified by MPLC (hexanes/EtOAc=1/0.5) to provide 5-allyl-7-methoxy-2-benzofuran-1(3H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-7bb85cd205b6421988145d2c88bfbcfe
Source noteuspto-grants-2015_04