HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879537Generated: October 26, 2026
Formaldehyde → 7-(benzyloxy)-N-methyl-9H-carbazol-2-amine
https://huagongshe.com/reaction/1879537
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 7-(benzyloxy)-9H-carbazol-2-amine | HCID 59282948 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-(benzyloxy)-N-methyl-9H-carbazol-2-amine | HCID 59283022 | 82.7% |
Reaction Steps
A mixture of 7-(benzyloxy)-9H-carbazol-2-amine (150 mg, 0.52 mmol), paraformaldehyde (78 mg, 2.6 mmol), and NaOMe (900 mg, 25% MeOH solution, 4.16 mmol) in 15 mL of MeOH was heated at reflux for 2 h under Ar atmosphere and cooled to rt. To this mixture was added NaBH4 (98 mg, 2.6 mmol) and the mixture was heated at reflux for 2 h. After cooling to rt, the mixture was quenched onto ice (30 g). It was extracted with EtOAc (3×50 mL) and the combined organic phase was dried over MgSO4 and concentrated. The crude product was purified with chromatography (hexane/EtOAc) to afford 7-(benzyloxy)-N-methyl-9H-carbazol-2-amine as a light-brown solid (130 mg, 82%). 1H NMR (400 MHz, acetone-d6) δ 9.78 (s, 1H), 7.72 (d, J=8.4 Hz, 1H), 7.66 (d, J=8.8 Hz, 1H), 7.49 (d, J=7.2 Hz, 2H), 7.37 (m, 2H), 7.32-7.28 (m, 1H), 6.98 (d, J=2.4 Hz, 1H), 6.78 (dd, J=8.4, 2.4 Hz, 1H), 6.56 (d, J=2.0 Hz, 1H), 6.49 (dd, J=8.4, 2.4 Hz, 1H), 5.13 (s, 2H), 4.96 (s, 1H), 2.82 (s, 3H); MS (ESI) m/z 303 (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-4885e2e86bd24a7cb881388f17aa627a |
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| Source note | uspto-grants-2012_11 |
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