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Sodium methanethiolate → HCID 63098091, 화합물

HRID 2408213
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HRID 2408213 반응식
[F:1][C:2]([F:9])([F:8])/[CH:3]=[CH:4]/[C:5]([OH:7])=[O:6].[CH3:10][S-:11].[Na+]>CO>[F:1][C:2]([F:9])([F:8])[CH:3]([S:11][CH3:10])[CH2:4][C:5]([OH:7])=[O:6]
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참가 물질

4

반응물 2

HCID 4378561Sodium methanethiolateHCID 57096144,4,4-Trifluorocrotonic acid

생성물 1

HCID 63098091HCID 63098091, 화합물수율 99.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a 100 mL round bottom flask was added (E)-4,4,4-trifluorobut-2-enoic acid (8 g, 57.1 mmol) and Methanol (24 mL), the solution was stirred in a water bath, then sodium methanethiolate (10.01 g, 143 mmol) was added in three portions. Vigorous bubbling was observed, the mixture was stirred at 25° C. overnight, NMR showed no more starting material. To the reaction mixture was added 2 N HCl until acidic. The mixture was extracted with chloroform (5×50 mL), combined organic layer was dried over Na2SO4, concentrated in vacuo and further dried under high vacuum until there was no weight loss to give 4,4,4-trifluoro-3-(methylthio)butanoic acid (10.68 g, 56.8 mmol, 99% yield) as a colorless oil: 1H NMR (400 MHz, CDCl3) δ 10.88 (s, 1H), 3.53 (dqd, J=10.5, 8.3, 4.0 Hz, 1H), 2.96 (dd, J=16.9, 4.0 Hz, 1H), 2.65 (dd, J=16.9, 10.4 Hz, 1H), 2.29 (s, 3H); 13C NMR (101 MHz, CDCl3) δ 175.78 (s), 126.61 (q, JC-F=278.8 Hz), 44.99 (q, JC-F=30.3 Hz), 34.12 (d, JC-F=1.7 Hz), 15.95 (s); EIMS m/z 162.

후처리

  1. customVigorous bubbling
  2. stirringthe mixture was stirred at 25° C. overnight
  3. additionTo the reaction mixture was added 2 N HCl until acidic
  4. extractionThe mixture was extracted with chloroform (5×50 mL)
  5. dry with materialwas dried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. customfurther dried under high vacuum until there

출처 및 근거

ORD 기록
ord-cd17ced9605542539d5ec422208c743a
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815271B2

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