Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 59282826 | HCID 59282826 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66933773 | HCID 66933773 | 100% |
Reaction Steps
To a suspension of 3-amino-6-(benzyloxy)-9H-carbazole 3 (90 mg, 0.31 mmol) and paraformaldehyde (47 mg, 1.57 mmol) in MeOH (20 mL) was added a solution of NaOMe in MeOH (0.32 mL, 1.56 mmol). The resulting mixture was heated at 80° C. for 1 h, then NaBH4 (59 mg, 1.55 mmol) was added. The resulting mixture was heated at 80° C. for 2 hrs, and then cooled to room temperature. To this solution was added NaOH (1 N, 30 mL). The mixture was then extracted with CH2Cl2 (3×20 mL). The combined organic layers were dried (MgSO4), filtered. The filtrate was concentrated in vacuo to give a brown solid (93 mg, 100%). It was used directly in the next step without any further purification. 1H NMR (acetone-d6, 400 MHz) δ: 9.68 (br s, 1H), 7.67 (d, J=2.4 Hz, 1H), 7.53 (d, J=7.6 Hz, 2H), 7.20-7.42 (m, 6H), 7.03 (dd, J=8.8, 2.4 Hz, 1H), 6.79 (dd, J=8.4, 2.4 Hz, 1H), 5.17 (s, 2H), 2.85 (s, 3H). MS: 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-0027cdf0694d4a45bf035cc67a1c7cb8 |
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| Source note | uspto-grants-2012_11 |
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