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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625840Generated: October 30, 2026

Ammonium Chloride → (4-Bromo-thiophen-2-yl)-(4-ethyl-phenyl)-methanol

https://huagongshe.com/reaction/1625840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
ReactantHCID 178436501HCID 178436501—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-thiophen-2-yl)-(4-ethyl-phenyl)-methanolHCID 64307567—

Reaction Steps

A solution of 4-bromo-2-thiophenecarboxaldehyde (4.78 g) in tetrahydrofuran (40 ml) was cooled to 0° C. under argon atmosphere, and thereto was added dropwise 4-ethylphenylmagnesium bromide (0.5 M tetrahydrofuran solution, 50 ml). The mixture was stirred at the same temperature for 30 minutes, and thereto was added a saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with brine and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=97:3-84:16) to give 4-bromo-2-thienyl-4-ethylphenylmethanol (5.37 g) as colorless oil. APCI-Mass m/Z 279/281 (M+H−H2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-951cbda088d14a35879b746b7020b566
Source noteuspto-grants-2014_07