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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739384Generated: November 1, 2026

Dimethylformamide → HCID 57229705, compound

https://huagongshe.com/reaction/1739384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant(1-Bromoethyl)benzeneHCID 11454—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86754603HCID 86754603—
SolventDiethyl EtherHCID 3283—
ProductHCID 57229705HCID 5722970591.3%

Reaction Steps

To a mixture of 0.25 g (1 mmol) of 5-(2-hydroxyiminomethyl-α-methoxybenzyl)-3-methylthiazole, 3 ml of N,N-dimethylformamide and 0.24 g (1.3 mmol) of α-methylbenzyl bromide was added 0.05 g (1.3 mmol) of 60% sodium hydride under ice-cooling and stirred at the same temperature for 3 hours. After completion of the reaction, 100 ml of ether was added and washed twice with 80 ml of brine. The ether layer was dried over anhydrous magnesium and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (ethyl acetate/n-hexane) to give 5-[α-methoxy-2-(4-phenyl-2-aza-3-oxa-1-pentenyl)benzyl]-3-methylthiazole (0.32 g, 91.3%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965740
Source datasetuspto-grants-1999_10
ORD IDord-848adbd8282048609416ad091ab545cc
Source noteuspto-grants-1999_10