HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355234Generated: October 30, 2026
Oxalyl chloride → HCID 178514620, compound
https://huagongshe.com/reaction/355234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 178514622 | HCID 178514622 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178514620 | HCID 178514620 | — |
Reaction Steps
To a solution of trans 3-azidocyclobutanecarboxylic acid (0.58 g, 4.1 mmol) in dichloromethane (10 ml) was added oxalyl chloride (0.45 ml) followed by one drop of N,N-dimethylformamide. The reaction mixture was stirred at 23° C. until the evolution of gas ceased (~2 h) and the solvent was evaporated in vacuo leaving a slightly yellow oil; 0.63 g, 95%; ir (neat) νmax : 2100 (N3) and 1785 cm-1 (C--O of acyl chloride); 1Hmr (CDCl3) δ: 4.12 (1H, m, H-1), 3.6 (1H, m, H-3) and 3.1-2.1 ppm (4H, H-2, H-4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04378314 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-95f23d5155734d1dbc67dee62be7cd47 |
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| Source note | uspto-grants-1983_03 |
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