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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728579Generated: October 31, 2026

Ethyl Bromide → HCID 15036289, compound

https://huagongshe.com/reaction/728579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantHCID 12284648HCID 12284648—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15036289HCID 15036289—

Reaction Steps

To a mixture of 9.5 g of metallic magnesium and 60 ml of diethyl ether was slowly added with stirring a solution of 43 g of ethyl bromide in 120 ml of diethyl ether. The mixed solution was heated for 15 minutes under refluxing and left to stand for cooling. The solution of ethylmagnesium bromide thus prepared above in ether was slowly added with stirring at inner temperature of below 10° C. to a solution of 7.5 g of 4-acetaminophthalide in 120 ml of tetrahydrofuran, followed by stirring at room temperature overnight. After the reaction was over, the reaction mixture was poured into aqueous ammonium chloride solution (saturated) under ice cooling and extracted twice with 400 ml of ethyl acetate. The combined extracts were concentrated to obtain an oily substance. The oily substance was purified by silica gel column chromatography to obtain 8.0 g of α,α-diethyl-2-hydroxymethyl-3-acetaminobenzyl alcohol in the colorness oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049575
Source datasetuspto-grants-1991_09
ORD IDord-7dbd196296d445e8b0df5226befd1158
Source noteuspto-grants-1991_09