HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → N-(4-Bromo-5,6,7,8-tetrahydronaphthalen-1-yl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-Acetamido-5,6,7,8-tetrahydronaphthalene | HCID 232065 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-(4-Bromo-5,6,7,8-tetrahydronaphthalen-1-yl)-acetamide | HCID 12710300 | 91.5% |
Reaction Steps
To a solution of compound 2A (2 g, 11 mmol) in AcOH (15 mL) cooled at 0° C. was added a solution of bromine (1.69 mL, 33 mmol) in AcOH (1.2 mL) slowly so that the reaction temperature was maintained below 17° C. After addition, the reaction mixture was stirred at rt until all the starting material was consumed (˜4 h). The reaction mixture was then poured into ice/water and the resulting suspension filtered. The collected solid was washed with H2O until the filtrate pH=6-7, and dried in a vacuum oven at 50° C. overnight to yield compound 2B (2.7 g) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405234B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-35d67dc2579f4147a0e9b3b15ee29a97 |
| Source note | uspto-grants-2008_07 |