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Water → 3,5-Difluoro-4-(methylthio)benzaldehyde

HRID 1838501
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HRID 1838501 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([F:11])[C:9]=1F)[CH:5]=[O:6].[CH3:12][S-:13].[Na+].O>C1COCC1>[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([F:11])[C:9]=1[S:13][CH3:12])[CH:5]=[O:6]
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참가 물질

5

반응물 3

HCID 962WaterHCID 27769543,4,5-TrifluorobenzaldehydeHCID 4378561Sodium methanethiolate

생성물 1

HCID 227466823,5-Difluoro-4-(methylthio)benzaldehyde수율 62.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 3,4,5-trifluorobenzaldehyde (30.0 g, 0.187 mol) in anhydrous THF (400 mL) cooled in a cold water bath was added sodium thiomethoxide (14.4 g, 0.20 mol) in portions over 30 minutes. The mixture was stirred at room temperature for 18 hours, then poured into water and extracted with dichloromethane (1×500 mL, 2×200 mL). The combined extracts were washed with water, dried using magnesium sulfate, and concentrated. Purification of the product by silica gel chromatography using 2% dichloromethane/5% ethyl acetate in hexanes gave the 3,5-difluoro-4-(methylthio)-benzaldehyde as a clear colorless liquid (22.0 g, 62%). 1H NMR (CDCl3/400 MHz) 9.86 (t, J=1.5, 1H), 7.34-7.39 (m, 2H), 2.55 (s, 3H). HRMS m/z 188.0099 (M+, calcd 188.0107).

후처리

  1. extractionextracted with dichloromethane (1×500 mL, 2×200 mL)
  2. washThe combined extracts were washed with water
  3. customdried
  4. concentrationconcentrated
  5. customPurification of the product by silica gel chromatography

출처 및 근거

ORD 기록
ord-af90c1147bbd4678abeee3270d8cbe4c
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06673818B2

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