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Methyl 4-bromo-2-methylbenzoate → Methyl 4-cyclobutyl-2-methylbenzoate

HRID 541270
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HRID 541270 반응식
[Br-].[CH:2]1([Zn+])[CH2:5][CH2:4][CH2:3]1.Br[C:8]1[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[C:10]([CH3:18])[CH:9]=1>>[CH:2]1([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[C:10]([CH3:18])[CH:9]=2)[CH2:5][CH2:4][CH2:3]1
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참가 물질

3

반응물 2

HCID 22031226Methyl 4-bromo-2-methylbenzoate2회HCID 178419766HCID 178419766, 화합물

생성물 1

HCID 10488418Methyl 4-cyclobutyl-2-methylbenzoate

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온도
65 °C

실험 절차

Cyclobutylzinc(II) bromide (50 ml, 0.5 M in THF, 25.0 mmol) was added to a mixture of methyl 4-bromo-2-methylbenzoate (compound 152.1, 5.2 g, 22.7 mmol) and PdCl2(dppf)CH2Cl2 (1.85 g, 2.27 mmol). The mixture was degassed and the flask was filled with argon through a balloon. The mixture was heated at 65° C. under argon for 24 hours. The mixture was cooled to 0° C. and quenched with water (10 ml). The mixture was diluted with EtOAc (200 ml), washed with water then with brine. The EtOAc layer was dried (Na2SO4), concentrated under reduced pressure, and purified using column (silica gel) chromatography (hexanes:EtOAc 30:1 to 20:1). Yield: 4.1 g, clear oil, 89.1%. 1H NMR (400 MHz, Chloroform-d) δ 7.86 (d, 1H), 7.12-7.02 (m, 2H), 3.88 (s, 3H), 3.59-3.48 (m, 1H), 2.59 (s, 3H), 2.35 (m, 2H), 2.22-1.96 (m, 3H), 1.86-1.84 (m, 1H).

후처리

  1. customThe mixture was degassed
  2. additionthe flask was filled with argon through a balloon
  3. temperatureThe mixture was cooled to 0° C.
  4. customquenched with water (10 ml)
  5. additionThe mixture was diluted with EtOAc (200 ml)
  6. washwashed with water
  7. dry with materialThe EtOAc layer was dried (Na2SO4)
  8. concentrationconcentrated under reduced pressure
  9. custompurified

출처 및 근거

ORD 기록
ord-27c91103071f4ea8a07639c0cc26aa8e
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871790B2

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