HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032499Generated: November 1, 2026
Ammonia → 8-(2-Furyl)-1,1,1,8-tetramethoxy-5-octyne
https://huagongshe.com/reaction/1032499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | Trimethyl 4-bromoorthobutyrate | HCID 5187924 | — |
| Reactant | 4-(2-Furyl)-4-methoxy-1-butyne | HCID 14774423 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(2-Furyl)-1,1,1,8-tetramethoxy-5-octyne | HCID 22166138 | 120.9% |
Reaction Steps
To a stirred solution of 4.09 g of lithium amide and 200 ml of liquid ammonia was added dropwise a solution of 24.3 g of 4-(2-furyl)-4-methoxy-1-butyne in 20 ml of tetrahydrofuran during 10 minutes. The mixture was stirred under reflux for 30 minutes and then treated dropwise with a solution of 40.4 g of 1-bromo-4,4,4-trimethoxybutane (U.S. Pat. No. 3,864,387) in 40 ml of tetrahydrofuran during 10 minutes. This solution was stirred under reflux for 60 minutes, the ammonia was allowed to evaporate over one hour and the resulting solution stirred at 20° C. for 10 minutes. The solution was then partitioned between ether and water, the organic layer separated, washed with brine, dried and concentrated, giving 58 g of crude 8-(2-furyl)-1,1,1,8-tetramethoxy-5-octyne as a liquid.
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-06fbead8ec41433f996633ea0357d336 |
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| Source note | uspto-grants-1990_09 |
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