HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 18518692, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 23567164 | HCID 23567164 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18518692 | HCID 18518692 | — |
Reaction Steps
The sub-title compound was prepared according to the method described in Example 10(ii) above from 7-methoxytetralin-1-yl-carboxylic acid, methyl ester (0.80 g; 3.6 mmol; see Example 10(i) above), NaH (55% in oil; 0.23 mg; 5.4 mmol), and allyl bromide (0.65 g, 5.4 mmol), whereafter the crude product was hydrolysed directly according to the method described in Example 10(iii) above with KOH (3 g) in EtOH:H2O (40 mL; 1:1). Yield 0.39 g (44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06576657B2 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-3bdd8c09f0ed4e95b42a9cbe98449ed4 |
| Source note | uspto-grants-2003_06 |