HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 21288490, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 21280500 | HCID 21280500 | — |
| Product | HCID 21288490 | HCID 21288490 | — |
Reaction Steps
For compounds in which X is --NR2 --(CHR1)n --, the corresponding amino starting compounds are employed to form the desired amino compound. Thus, aniline is condensed with 3-(1-hydroxyhexyl)benzylbromide to form 2-[3-(1-hydroxyhexyl)benzylamino]benzene. Alternatively, benzyl bromide is condensed with 3-(1-hydroxyhexyl)aniline to form 2-[3-(1-hydroxyhexyl)anilinomethyl]benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04778931 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-92042b8a8b384e9c9c692acae5cb02c7 |
| Source note | uspto-grants-1988_10 |