HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Tert-butyl 3-(methylamino)benzylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | tert-butyl N-((3-aminophenyl)methyl)carbamate | HCID 10775412 | — |
| Product | Tert-butyl 3-(methylamino)benzylcarbamate | HCID 57763264 | — |
Reaction Steps
Tert-butyl 3-aminobenzylcarbamate was converted to the target molecule following standard reductive amination conditions using formaldehyde and sodium cyanoborohydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504420B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-fbc5cb693c1a4ee4ad60661f5959feb5 |
| Source note | uspto-grants-2009_03 |