HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032504Generated: October 31, 2026
Ammonia → 2,5-Dihydro-2,5-dimethoxy-2-(8,8,8-trimethoxy-3-octynyl)furan
https://huagongshe.com/reaction/1032504
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | Trimethyl 4-bromoorthobutyrate | HCID 5187924 | — |
| Reactant | 2,5-Dihydro-2,5-dimethoxy-2-(3-butynyl)furan | HCID 14774426 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,5-Dihydro-2,5-dimethoxy-2-(8,8,8-trimethoxy-3-octynyl)furan | HCID 22166145 | 108.2% |
Reaction Steps
To a stirred mixture of 0.51 g of lithium amide and ml of liquid ammonia was added dropwise a solution of 3.64 g of 2,5-dihydro-2,5-dimethoxy-2-(3-butynyl)furan in 2.5 ml of tetrahydrofuran during 5 minutes. The mixture was stirred under reflux for 30 minutes and then treated dropwise with a solution of 5.0 g of 1-bromo-4,4,4-trimethoxybutane (U.S. Pat. No. 3,864,387) in 5 ml of tetrahydrofuran during 5 minutes. This solution was stirred under reflux for one hour, the ammonia allowed to evaporate during one hour and the resulting solution stirred at 20° C. for 10 minutes. This solution was partitioned with ether and brine. The organic layer was dried, treated with 2 drops of pyridine, and then concentrated, giving 7.1 g of the desired compound as a light amber oil; PMR δ 5.9 (2H, m, vinyl hydrogens).
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-ade4828b740c429e9484a8d1b2ed028f |
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| Source note | uspto-grants-1990_09 |
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