HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 7-bromo-3,3-dimethyl-3,4-dihydro-2H-benzo[b][1,4]dioxepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 19935415 | HCID 19935415 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-bromo-3,3-dimethyl-3,4-dihydro-2H-benzo[b][1,4]dioxepine | HCID 19935531 | 108.2% |
Reaction Steps
8.55 g of 3,4-dihydro-3,3-dimethyl-2H-1,5-benzodioxepine (see Example 10) were dissolved in 70 ml of methylene chloride (CH2Cl2) and treated at 0° C. under an Argon atmosphere with a solution of 8.0 g of Br2 in 30 ml of CH2Cl2. The mixture was warmed to room temperature and left to react for 1 hour. It was then poured on to ice and extracted with ether. Washing with NaHCO3 solution and water, drying and evaporation yielded 13.35 g of 7-bromo-3,4-dihydro-3,3-dimethyl-2H-1,5-benzodioxepine as a colorless oil which was 94.5% pure and which contained 4.7% of starting material; it was processed in the crude state.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420273 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-86e367df791e43c89c0c9f5ccfdbced5 |
| Source note | uspto-grants-1995_05 |