HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminobenzyl alcohol → 2-Amino-5-bromobenzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminobenzyl alcohol | HCID 21439 | — |
| Reactant | 2,4,4,6-Tetrabromocyclohexa-2,5-dienone | HCID 88433 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Amino-5-bromobenzenemethanol | HCID 11030874 | — |
Reaction Steps
To a solution of 2-aminobenzyl alcohol (7.12 g, 58 mmol) in methylene chloride (200 mL) at −10° C., 2,4,4,6-tetrabromo-2,5-cyclohexadien-1-one (25 g, 61 mmol) was added in portions. During the addition, the temperature of the reaction mixture was maintained between −10° C. and 0° C. The reaction mixture was warmed up to room temperature and then extracted with 2 N sodium hydroxide solution (2×50 mL). The organic layer was washed with water and dried over MgSO4, filtered and concentrated in vacuo to afford 2-amino-5-bromobenzylalcohol as a yellow solid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06884782B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-e00c413433924070b07403214a83ec1d |
| Source note | uspto-grants-2005_04 |