HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 3-Benzyloxyaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-Nitrophenol | HCID 11137 | — |
| Reactant | 3-Fluorobenzyl bromide | HCID 68007 | — |
| Product | 3-Benzyloxyaniline | HCID 92892 | — |
Reaction Steps
3-Nitro-phenol was reacted with bromomethyl-benzene according to the procedure from Example 199A substituting bromomethyl-benzene for 1-bromomethyl-3-fluoro-benzene then reduced according to the procedure from Example 199B to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915411B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-6198c75e4d9d476491564a7a5aa76fbd |
| Source note | uspto-grants-2011_03 |