HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032498Generated: November 1, 2026
Propargyl bromide → 4-(2-Furyl)-4-methoxy-1-butyne
https://huagongshe.com/reaction/1032498
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | 2-(Dimethoxymethyl)furan | HCID 11815465 | — |
| Reactant | Propargyl aluminum bromide | HCID 86744225 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-Furyl)-4-methoxy-1-butyne | HCID 14774423 | — |
Reaction Steps
To a stirred solution of propargyl aluminum bromide, prepared from 52.9 g of 80% propargyl bromide in toluene, 6.41 g of aluminum splutters activated with 70 mg of mercuric choride and 80 ml of tetrahydrofuran, was added dropwise a solution of 42.2 g of furfural dimethyl acetal [J. Org. Chem., 40, 1478 (1975)] in 30 ml of tetrahydrofuran during a 15 minute period while maintaining a temperature of. 25° to 30° C. The mixture was stirred for 20 minutes at 25° C., then partitioned with ether and ice-water. The organic layer was separated, washed with water, then aqueous sodium bicarbonate, finally with brine and dried. After evaporation the residue was distilled, giving 39.8 g of the desired compound, bp 68°-69° C. (11 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04958037 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-b993ba9142e94eea8bd5cbcb62f1af6c |
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| Source note | uspto-grants-1990_09 |
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