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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607654Generated: October 31, 2026

Methanol → 7-[(Butan-2-yl)oxy]-5-methoxy-2,2-dimethyl-2H-1-benzopyran

https://huagongshe.com/reaction/1607654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70381861HCID 70381861—
SolventTetrahydrofuranHCID 8028—
Product7-[(Butan-2-yl)oxy]-5-methoxy-2,2-dimethyl-2H-1-benzopyranHCID 18533085%

Reaction Steps

In a mixture of 60 ml of tetrahydrofuran and 40 ml of methanol 5.6 g (20 millimoles) of 5-methoxy-7-sec. butoxy-2,2-dimethyl-4-chromanone are dissolved, whereupon 1.5 g (40 millimoles) of sodium tetrahydroborate are added in small portions and the reaction mixture is heated to boiling for 2 hours. The reaction mixture is worked up according to Example 31. The product is purified by column chromatography. Thus 4.4 g of the desired compound are obtained in the form of a light yellow oil, yield 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866089
Source datasetuspto-grants-1989_09
ORD IDord-89f3d7965cf04c1e9f546276cf827b07
Source noteuspto-grants-1989_09