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Azobisisobutyronitrile → HCID 14820509, 화합물

HRID 1088729
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HRID 1088729 반응식
[OH:1][C:2]1[C:3]([CH2:11][CH:12]=[CH2:13])=[CH:4][C:5]2[S:9][CH2:8][CH2:7][C:6]=2[CH:10]=1.CC(N=NC(C#N)(C)C)(C#N)C.[C:26]1([SH:32])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>C(=O)(O)[O-].[Na+]>[OH:1][C:2]1[C:3]([CH2:11][CH2:12][CH2:13][S:32][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[CH:4][C:5]2[S:9][CH2:8][CH2:7][C:6]=2[CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 7969ThiophenolHCID 14820507HCID 14820507, 화합물

생성물 1

HCID 14820509HCID 14820509, 화합물

시약·촉매·용매 1

HCID 516892Sodium Bicarbonate용매

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온도
90 °C

실험 절차

To a solution of 5-hydroxy-6-allyl-2,3-dihydrobenzothiophene (125 mg, 0.65 mmole) in 0.5 mL thiophenol was added 28 mg AIBN. The reaction mixture was purged with nitrogen and heated to 90° C. for 3 hours. TLC analysis (90/10 hexane/EtOAc) showed the reaction to be complete. The reaction mixture was diluted with 25 mL saturated sodium bicarbonate and extracted 3×25 mL EtOAc. The combined organics were washed with sodium bicarbonate (2×25 mL), H2O (1×25 mL) and brine (1×25 mL). Drying over Na2SO4, filtration and concentration afforded 568 mg crude product as an oil. Purification by flash chromatography (90/10, hexane/EtOAc) 126 mg (64%) pure product NMR 287 MS181.

후처리

  1. customThe reaction mixture was purged with nitrogen
  2. customthe reaction
  3. extractionextracted 3×25 mL EtOAc
  4. washThe combined organics were washed with sodium bicarbonate (2×25 mL), H2O (1×25 mL) and brine (1×25 mL)
  5. dry with materialDrying over Na2SO4, filtration and concentration

출처 및 근거

ORD 기록
ord-eb4b33dc41cf49bf8a81edf437f616f9
출처 데이터셋
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04963580

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