HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 14155410, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | (2-Amino-3-chlorophenyl)methanol | HCID 14155407 | — |
| Product | HCID 14155410 | HCID 14155410 | — |
Reaction Steps
This material was prepared from 2-amino-3-chlorobenzyl alcohol and benzyl bromide by the general procedure outlined in Example 98. The product was purified by Kugelrohr distillation to yield an oil, b.p. 118°-125° C. (0.1 mm). The product was characterized by IR and 1H NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04886883 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-33f884f803704c0cbdd50acdd5c32a65 |
| Source note | uspto-grants-1989_12 |