HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Benzotriazole-1-carboxaldehyde → HCID 86585982, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Benzotriazole-1-carboxaldehyde | HCID 576740 | — |
| Reactant | HCID 69949710 | HCID 69949710 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86585982 | HCID 86585982 | 88.9% |
Reaction Steps
A stirred mixture of the product from Step 9 (0.39 g, 0.93 mmol) and THF (15 ml), under nitrogen is treated with N-formylbenzotriazole (0.164 g, 1.12 mmol) and kept at ambient temperature for 1 h. It is then concentrated in vacuo. Chromatography of the residue on silica gel with mixtures of acetone-methylene chloride containing 20-40% acetone gave 0.37 g of the titled product: 1H NMR (300 MHz, CDCl3) δ0.00 (m, 6H), 0.73, 0.86 (s, s, 9H), 2.02 (s, 3H), 2.70, 3.23 (m, m, 2H), 3.68 (m, 5H), 4.03 (m, 1H), 4.43, 4.80 (m, m, 1H), 4.75 (m, 1H), 6.14 (m, 1H), 7.08, 7.20, 7.47, 7.61, 8.04 (m, 3H), 8.52, 8.86 (s, s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06387896B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-d862bdba76294e9ba1208c0b8555d8ae |
| Source note | uspto-grants-2002_05 |