Bromine → 4-Acetamido-3-bromo-2,6-dimethylanisole

HRID 1488452

반응식

HRID 1488452 반응식
[C:1]([NH:4][C:5]1[CH:10]=[C:9]([CH3:11])[C:8]([O:12][CH3:13])=[C:7]([CH3:14])[CH:6]=1)(=[O:3])[CH3:2].[Br:15]Br>C(O)(=O)C>[C:1]([NH:4][C:5]1[CH:10]=[C:9]([CH3:11])[C:8]([O:12][CH3:13])=[C:7]([CH3:14])[C:6]=1[Br:15])(=[O:3])[CH3:2]

참가 물질

4

반응물 2

HCID 24408BromineHCID 218527644-Acetamido-2,6-dimethylanisole

생성물 1

HCID 229056464-Acetamido-3-bromo-2,6-dimethylanisole수율 85.4%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

4-Acetamido-2,6-dimethylanisole (7, 8.6 g, 44.3 mmol) and acetic acid (30 mL) were placed in a round-bottom flask under an argon atmosphere. Bromine (2.7 mL, 44.3 mmol) was added dropwise to the solution, after which the reaction mixture was stirred at room temperature for about 3 h, and then concentrated. The residue was diluted with methylene chloride and carefully washed sequentially with saturated aq. sodium bicarbonate and brine, and dried (MgSO4). Removal of solvents gave a brown-colored solid which was recrystallized from methylene chloride-hexanes to yield 4-acetamido-3-bromo-2,6-dimethylanisole (10.3 g, 85% yield) as an off-white solid, mp 152°-153° C. Spectral data: 1H NMR: δ 2.18 (s, 3H), 2.24 (s, 3H), 2.35 (s, 3H), 3.66 (s, 3H), 7.55 (br s, 1H), 7.9 (s, 1H); 13C NMR: δ 16.1, 16.8, 24.6, 60.1, 114.5, 122.0, 130.5, 131.3, 131.5, 153.6, 168.1; CI-HRMS: calcd. for C11H15BrNO2 (M+H+) 272.0286, fnd. 272.0284.

후처리

  1. concentrationconcentrated
  2. additionThe residue was diluted with methylene chloride
  3. washcarefully washed sequentially with saturated aq. sodium bicarbonate and brine
  4. dry with materialdried (MgSO4)
  5. customRemoval of solvents
  6. customgave a brown-colored solid which
  7. customwas recrystallized from methylene chloride-hexanes

출처 및 근거

ORD 기록
ord-2c3c29bb2b8f421d8649d202e963792b
출처 데이터셋
uspto-grants-1997_10
특허 번호
US05674876

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