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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534375Generated: November 2, 2026

Sodium borohydride → HCID 15694369, compound

https://huagongshe.com/reaction/1534375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15703848HCID 15703848—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15694369HCID 15694369—

Reaction Steps

158 g (0.41 mmol) of 3-(3-methyl-1-butanonyl)-4,11-dimethoxy-9-methyl-7H-dibenzo[b,g][1,5]dioxocin-5-one are dissolved in 2 ml of tetrahydrofuran and 0.1 ml of water. 23 mg (0.61 mmol) of sodium borohydride are added to the solution and the mixture is stirred overnight at room temperature. Excess sodium borohydride is destroyed by addition of a few drops of acetic acid. The mixture is concentrated in vacuo, the residue is taken up in dichloromethane and the solution is washed with water. The organic phase is dried over magnesium sulphate, concentrated and purified by column chromatography on silica gel using petroleum ether/diethyl ether 1:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089487
Source datasetuspto-grants-1992_02
ORD IDord-0e7e537f72c0439ba070309542d66de9
Source noteuspto-grants-1992_02