HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Bromo-1-[8-(tert-butyl)-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-6-yl]-1-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-[8-(tert-Butyl)-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-6-yl]-1-ethanone | HCID 58910032 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Bromo-1-[8-(tert-butyl)-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-6-yl]-1-ethanone | HCID 58909948 | 13% |
Reaction Steps
1-(8-tert-Butyl-4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)ethanone (250 mg, purchased from Chembiotek, India) was warmed to 50° C. to 55° C. in a mixture of acetic acid (4 ml) and toluene (8 ml). Bromine (200 mg dissolved in acetic acid) was carefully added dropwise at this temperature. After 2.5 h, the heating was removed, and the mixture was treated with ice water at RT and extracted three times with toluene. The combined organic phases were dried over sodium sulfate, filtered and concentrated. The crude product was purified on silica gel, so that 65 mg of the desired compound were obtained, in addition to a further 43 mg of product, which were slightly contaminated, and 37 mg of starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863269B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-f2e4196a1a78498c8d481a8fa0b71c24 |
| Source note | uspto-grants-2011_01 |