Triphenylphosphine → 4-(2-Chloroethyl)-4,5,6,7-tetrahydrobenzo[b]thiophene

HRID 1516938노트

반응식

HRID 1516938 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[S:20]1[CH:24]=[CH:23][C:22]2[CH:25]([CH2:29][CH2:30]O)[CH2:26][CH2:27][CH2:28][C:21]1=2.C(Cl)(Cl)(Cl)[Cl:33].C(#N)C>>[Cl:33][CH2:30][CH2:29][CH:25]1[C:22]2[CH:23]=[CH:24][S:20][C:21]=2[CH2:28][CH2:27][CH2:26]1

참가 물질

4

실험 절차

Triphenylphosphine (3.94 g, 15 mmol) is added to a solution of 2-(4,5,6,7-tetrahydrobenzo[b]thiophen-4-yl)ethanol (2.74 g, 15 mmol) in Cl4C/Acetonitrile 1:1 (20 mL) at room temperature and the mixture is maintained under stirring for 3 hours monitoring the reaction by TLC. The solution is concentrated to half the volume at reduced pressure, CH2Cl2 is added and washed with water. The organic phase is separated and evaporated to dryness. The crude is treated with diethyl ether and the precipitate is filtered. The diethyl ether is evaporated to dryness, and the resulting crude is purified by column chromatography, giving 4-(2-chloroethyl)-4,5,6,7-tetrahydrobenzo[b]thiophene (1.7 g, 8.4 mmol, 56%, oil). 1H NMR (300 MHz, CDCl3): δ 1.54 (m, 1H), 1.79 (m, 1H), 1.92 (m, 3H), 2.20 (m, 1H), 2.77 (m, 2H), 3.00 (m, 1H), 3.64 (m, 2H), 6.86 (d, J=5.2 Hz, 1H), 7.06 (d, J=5.2 Hz, 1H).

후처리

  1. temperaturethe mixture is maintained
  2. customthe reaction by TLC
  3. concentrationThe solution is concentrated to half the volume at reduced pressure, CH2Cl2
  4. additionis added
  5. washwashed with water
  6. customThe organic phase is separated
  7. customevaporated to dryness
  8. additionThe crude is treated with diethyl ether
  9. filtrationthe precipitate is filtered
  10. customThe diethyl ether is evaporated to dryness
  11. customthe resulting crude is purified by column chromatography

출처 및 근거

ORD 기록
ord-64ec361d5ec847a793a347187d21724c
출처 데이터셋
uspto-grants-2012_07
특허 번호
US08227625B2

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