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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439787Generated: October 29, 2026

Benzaldehyde → HCID 67744360, compound

https://huagongshe.com/reaction/439787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantMethanol--water (1/1)HCID 22242641—
ReactantHCID 22408116HCID 22408116—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 67744360HCID 67744360—

Reaction Steps

2-(4-Bromo-3-methylbenzyloxy)tetrahydropyran (1.4 g, 5 millimol) was dissolved in tetrahydrofuran (5ml), and cooled to -20° C. with methanol-water. Under nitrogen atmosphere, thereto was added 15% hexane solution (5 ml) of n-butyllithium, and in this state, the mixture was stirred for 30 minutes. Next, benzaldehyde (0.6 ml, 6 millimol) was added, and stirred for 2 hours. During this procedure, inner-temperature was raised from -20° C. to 30° C. Then, water was added, and the mixture was extracted with ethyl acetae. After washing with water and saturated aqueous sodium chloride solution, the solvent was distilled away, and the residue was separated and purified by using a silica-gel column chromatography (ethyl acetatee:n-hexane=1:5 to 1:2) to give the title compound (0.9 g, 2.9 millimol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516777
Source datasetuspto-grants-1996_05
ORD IDord-6432981ac9264a4f86a0d5be0cb2fa0a
Source noteuspto-grants-1996_05