HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 25072816, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 25072815 | HCID 25072815 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 25072816 | HCID 25072816 | — |
Reaction Steps
1-(Phenylsulfonyl)-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol, Example 15 (34.4 mg, 0.11 mmol) was dissolved in DME (2 mL) and added formaldehyde (37% Wt. solution in water, 0.1 mL, 1.1 mmol), acetic acid (0.05 mL, 0.7 mmol) and sodium triacetoxyborohydride (156 mg, 0.7 mmol). The reaction mixture was stirred at room temperature for 24 H. The reaction was quenched by adding 1 M NaOH (5 mL). Aqueous phase (pH about 14) was separated and was then extracted with DCM (3×5 mL). The combined organic phases was washed with water and brine, and dried with MgSO4. The solvent was removed under vacuum. 20 mg pure product was obtained as an off-white solid. MS m/z 327 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138333B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-9d043d59ecb14a1f9638ab6ecb3e4818 |
| Source note | uspto-grants-2012_03 |