HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249612Generated: November 2, 2026
Methyl propiolate → HCID 17878067, compound
https://huagongshe.com/reaction/249612
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl propiolate | HCID 13536 | — |
| Reactant | Benzene, 1,1',1''-(azidomethylidyne)tris- | HCID 84340 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 17878067 | HCID 17878067 | 62% |
Reaction Steps
To a suspension of sodium azide (19.0 g : 0.283 Mol.) in dimethyl- formamide (130 ml) is added trityl chloride (76.0 g : 0.273 Mol.), and the mixture is stirred at room temperature for 5 hours. The reaction mixture is diluted with water and extracted with ether. The extract is washed with brine, dried over sodium sulfate, and concentrated to give trityl azide. To a solution of this azide in acetone (300 ml) is added methyl propiolate (24 ml : 0.27 Mol.), and the mixture is heated under reflux for 6 days. The reaction mixture is cooled to the room temperature and diluted with ether. The separating crystals are collected by filtration to give 1-trityl-1,2,3-triazol-4-ylcarboxylic acid methyl ester (62.0 g) as colorless crystals. Yield: 62%. mp. 189° to 190° C. NMR δ (CDCl3) ppm: 3.93(s, 3H), 7.05-7.15(m, 6H), 7.3-7.4(m, 9H), 8.02(s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214037 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-fae735354a4a412b923647abaab0c635 |
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| Source note | uspto-grants-1993_05 |
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