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Trimethyl orthoformate → Methyl 3-chloro-2-methylbenzoate

HRID 915354
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HRID 915354 반응식
[Cl:1][C:2]1[C:3]([CH3:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[CH:12](OC)(OC)OC>CO>[CH3:12][O:6][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][CH:10]=[C:2]([Cl:1])[C:3]=1[CH3:11]
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참가 물질

4

반응물 2

HCID 9005Trimethyl orthoformateHCID 820103-Chloro-2-methylbenzoic acid

생성물 1

HCID 5077673Methyl 3-chloro-2-methylbenzoate수율 96.1%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
60 °C

실험 절차

Alternatively, to a suspension of 3-chloro-2-methylbenzoic acid (6.8 g, 40 mmol) in methanol (40 mL) was added trimethyl orthoformate (4.4 mL, 40 mmol). HCl gas was then bubbled through the suspension for 20 minutes. The resulting solution was then heated in a 60° C. oil bath. After stirring at 60° C. for 16 hours, the solution was allowed to cool to ambient temperature and concentrated under reduced pressure to afford a thick yellow paste. The semi-solid was melted under reduced pressure using a heat gun, and then cooled to afford 3-chloro-2-methylbenzoic acid methyl ester (7.1 g, 95% yield) as a yellow crystalline solid: 1H-NMR (400 MHz, CDCl3): δ 7.70 (1H, d, J=7.8 Hz), 7.51 (1H, d, J=7.8 Hz), 7.17 (1H, t, J=7.8 Hz), 3.91 (s, 3H), 2.60 (s, 3H) ppm.

후처리

  1. customHCl gas was then bubbled through the suspension for 20 minutes
  2. temperatureto cool to ambient temperature
  3. concentrationconcentrated under reduced pressure
  4. customto afford a thick yellow paste
  5. temperaturecooled

출처 및 근거

ORD 기록
ord-a29b57fe62964f598d0686b5e8f8f0f3
출처 데이터셋
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07265131B2

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