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Water → 5-Cyano-2,3-dihydro-3,3-dimethyl-2-isothiocyanatobenzofuran

HRID 444087
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HRID 444087 반응식
Cl[CH:2]1[C:6]([CH3:8])([CH3:7])[C:5]2[CH:9]=[C:10]([C:13]#[N:14])[CH:11]=[CH:12][C:4]=2[O:3]1.[S-:15][C:16]#[N:17].[K+].O>CN(C)C=O>[C:13]([C:10]1[CH:11]=[CH:12][C:4]2[O:3][CH:2]([N:17]=[C:16]=[S:15])[C:6]([CH3:8])([CH3:7])[C:5]=2[CH:9]=1)#[N:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 516872Potassium thiocyanateHCID 205362092-Chloro-5-cyano-2,3-dihydro-3,3-dimethylbenzofuran

생성물 1

HCID 205362295-Cyano-2,3-dihydro-3,3-dimethyl-2-isothiocyanatobenzofuran수율 21.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2-Chloro-5-cyano-2,3-dihydro-3,3-dimethylbenzofuran (5 g) from Example 15 and potassium thiocyanate (4.6 g) were heated in dimethylformamide (30 ml) at 110° C. for 7 hours. The mixture, after cooling, was added to water and the product extracted into diethyl ether. The ether solution was washed with water (twice), dried over magnesium sulphate and run down under vacuum yielding 4 g of crude product. Purification by silica gel chromatography in toluene yielded 1.2 g of title product, mp 52° C.

후처리

  1. temperatureThe mixture, after cooling
  2. extractionthe product extracted into diethyl ether
  3. washThe ether solution was washed with water (twice),
  4. dry with materialdried over magnesium sulphate
  5. customyielding 4 g of crude product
  6. customPurification by silica gel chromatography in toluene

출처 및 근거

ORD 기록
ord-632947a72b384ee4833bda6bef6d884f
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04263037

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