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Acetic Anhydride → Acetic acid 1-methyl-1-(2-methyl-pyridin-3-yl)-ethyl ester

HRID 250959
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HRID 250959 반응식
[CH3:1][C:2]1[C:7]([C:8]([OH:11])([CH3:10])[CH3:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[CH3:12][C:13](OC(C)=O)=[O:14]>CN(C1C=CN=CC=1)C>[CH3:10][C:8]([O:11][C:13](=[O:14])[CH3:12])([C:7]1[C:2]([CH3:1])=[N:3][CH:4]=[CH:5][CH:6]=1)[CH3:9]
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참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 450917322-(2-Methylpyridin-3-yl)propan-2-ol

생성물 1

HCID 67272080Acetic acid 1-methyl-1-(2-methyl-pyridin-3-yl)-ethyl ester수율 75%

시약·촉매·용매 1

HCID 142844-(Dimethylamino)pyridine촉매

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온도
100 °C

실험 절차

2-(2-methyl-pyridin-3-yl)-propan-2-ol (1.30 g, 8.61 mmol) and DMAP (30 mg) were combined in Ac2O (8 mL) and stirred at 100° C. for 16 hours. Following removal of the solvent under reduced pressure, the brown residue was quenched with saturated NaHCO3 (50 mL) and extracted with CH2Cl2 (5×60 mL). The combined organic extracts were dried (Na2SO4), filtered, and concentrated in vacuo to afford a yellow oil. Purification via column chromatography on silica gel (CH2Cl2:MeOH, 95:5, v/v) afforded acetic acid 1-methyl-1-(2-methyl-pyridin-3-yl)-ethyl ester as a white crystalline solid (1.25 g, 75%). 1H NMR (CDCl3) δ 1.80 (s, 3H), 2.05 (s, 3H), 2.66 (s, 3H), 7.12 (dd, 1H, J=9.0, 6.0 Hz), 7.62 (dd, 1H, J=9.0, 3.0 Hz), 8.39 (dd, 1H, J=6.0, 3.0 Hz).

후처리

  1. customremoval of the solvent under reduced pressure
  2. customthe brown residue was quenched with saturated NaHCO3 (50 mL)
  3. extractionextracted with CH2Cl2 (5×60 mL)
  4. dry with materialThe combined organic extracts were dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto afford a yellow oil
  8. customPurification via column chromatography on silica gel (CH2Cl2

출처 및 근거

ORD 기록
ord-42ef7f2f8b394e13a6fd16874ad84ee4
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863293B2

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