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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968866Generated: November 2, 2026

Water → 1-Bromo-4-(1-propynyl)benzene

https://huagongshe.com/reaction/1968866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantBenzene, 1-bromo-4-ethynyl-HCID 136603—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-4-(1-propynyl)benzeneHCID 575587—

Reaction Steps

To a solution of 1-bromo-4-ethynyl-benzene (500 mg, 2.8 mmol) in tetrahydrofuran (20 mL) at −30° C. was slowly added sodium bis(trimethylsilyl)amide in tetrahydrofuran solution (1M, 4.2 mL). After stirring 15 min, methyl iodide (1.1 g, 8.4 mmol) was added at −20° C. The resulting reaction mixture was stirred at RT for 50 min before it was added to water. The mixture was extracted with ethyl acetate and the organic phase was dried over magnesium sulfate and concentrated. The crude product 1-bromo-4-prop-1-ynyl-benzene was obtained as a volatile liquid (450 mg, 82.8% yield) which was put to next step directly without further purification. 1H NMR (400 MHz, MeOD) δ ppm 7.34 (d, J=8.3 Hz, 10H), 7.14 (d, J=8.3 Hz, 10H), 1.91 (s, 3H); GCMS, (M+1)=195.1, Molecular Formula=C9H7Br.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426414B2
Source datasetuspto-grants-2013_04
ORD IDord-4a9cc71918ba42e9b0a3dd1220215038
Source noteuspto-grants-2013_04