HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 59242117, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Ethoxy-3-fluoroaniline | HCID 19599205 | — |
| Reactant | HCID 68516737 | HCID 68516737 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Product | HCID 59242117 | HCID 59242117 | — |
Reaction Steps
(4-Ethoxy-3-fluoro-phenyl)-methyl-amine hydrochloride: The free base of the title compound was synthesized as a clear, pale tan liquid by a procedure similar to that found in Example 221 from 4-ethoxy-3-fluoro-phenylamine (1.828 g, 11.78 mmol), 1H-benzotriazole (1.407 g, 11.8 mmol), 37 wt % aq formaldehyde (0.90 mL, 12.1 mmol) and sodium borohydride (447 mg, 11.8 mmol); with purification by MPLC (SiO2/0-33% EtOAc in hexanes). The title compound was obtained as an off-white solid after concentrating a soln of the free base in HCl-i-PrOH in vacuo. LC-MS (ESI+; 170 ([M+H]+)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309562B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-4e021e2338e44b24a957d777fb065319 |
| Source note | uspto-grants-2012_11 |