HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879538Generated: October 26, 2026
1,2-Dichloroethane → N-(7-(benzyloxy)-9H-carbazol-2-yl)-N-methylformamide
https://huagongshe.com/reaction/1879538
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | 7-(benzyloxy)-N-methyl-9H-carbazol-2-amine | HCID 59283022 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(7-(benzyloxy)-9H-carbazol-2-yl)-N-methylformamide | HCID 86651370 | 83.2% |
Reaction Steps
To 7-(benzyloxy)-N-methyl-9H-carbazol-2-amine (120 mg, 0.4 mmol), formic acid (55 mg, 1.2 mmol) and DMAP (5 mg, 0.04 mmol) in 3 mL of pyridine was added portionwise EDC (230 mg, 1.2 mmol). The mixture was stirred at rt for 3 h under Ar atmosphere and concentrated under reduced pressure. The residue was diluted with EtOAc (50 mL) and washed with water (2×50 mL), 0.5 M HCl(2×50 mL), and brine (50 mL), and dried over MgSO4. After solvent removal, the crude product was purified with chromatography (hexane/EtOAc) to afford N-(7-(benzyloxy)-9H-carbazol-2-yl)-N-methylformamide as a white solid (110 mg, 83%). 1H NMR (400 MHz, acetone-d6) δ 10.34 (s, 1H), 8.49 (s, 1H), 8.02 (d, J=8.4 Hz, 1H), 7.98 (d, J=8.8 Hz, 1H), 7.51 (d, J=7.2 Hz, 2H), 7.39 (m, 2H), 7.34-7.28 (m, 1H), 7.13 (d, J=2.4 Hz, 1H), 7.08 (dd, J=8.4, 2.4 Hz, 1H), 6.91 (dd, J=8.4, 2.4 Hz, 1H), 5.19 (s, 2H), 3.31 (s, 3H); MS (ESI) m/z 331 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318132B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-c667f0b812d1498790f91a4fb4ea1359 |
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| Source note | uspto-grants-2012_11 |
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