HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Benzyloxy)-3-bromobenzene → HCID 18980432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Benzyloxy)-3-bromobenzene | HCID 2756638 | — |
| Reactant | HCID 18980424 | HCID 18980424 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | HCID 18980432 | HCID 18980432 | 65% |
Reaction Steps
1-bromo-3-benzyloxy-benzene and the base of compound (42) were reacted corresponding to the conditions described in Example 1. The product obtained was dissolved in ether/hexane and the base was extracted with 10% acetic acid. After adjusting to an alkaline pH, compound (43) was extracted with ether and dried over sodium sulphate. After removing the solvent by distillation the product was purified with 1:1 ether/diisopropyl ether via an alumina column (3.6% water). Compound (43) was obtained in a yield of 65% theoretical.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05801201 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-f3631254511e4fb097a8b60f1e2a6805 |
| Source note | uspto-grants-1998_09 |