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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491746Generated: October 31, 2026

Iodoethane → 7-Ethyl-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole

https://huagongshe.com/reaction/491746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant7-Bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazoleHCID 12148969—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product7-Ethyl-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazoleHCID 1148296691%

Reaction Steps

n-Butyllithium (2.5 N, 0.43 mL, 1.08 mmol) was added dropwise into a cold (−78° C.) mixture of 7-bromo-5-methoxy-2-(4-methoxyphenyl)-1,3-benzoxazole (300 mg, 0.90 mmol) and THF (2 mL). The mixture was allowed to stir for 0.5 h. Iodoethane (0.14 mL, 1.8 mmol) was added dropwise into the mixture. The reaction mixture was allowed to warm to room temperature and stirred for 2 h. The reaction was quenched with aqueous ammonium chloride, poured into water, and extracted with EtOAc. The organic extracts were washed with brine and dried over MgSO4. Evaporation and flash chromatography (20% EtOAc/petroleum ether) gave (231 mg, 91% yield) of the product as a light brown solid: m.p. 85° C.; MS m/e 284 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531564B2
Source datasetuspto-grants-2009_05
ORD IDord-1346cc4e34af4b6584e9a4e01ce0ae14
Source noteuspto-grants-2009_05