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Tetrabutylammonium Fluoride → 3-(2-tert-butylphenyl)-1H-indole

HRID 2423218
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반응식

HRID 2423218 반응식
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13](S(C2C=CC=CC=2)(=O)=O)[CH:12]=1)([CH3:4])([CH3:3])[CH3:2].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][CH:12]=1)([CH3:4])([CH3:2])[CH3:3]
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참가 물질

4

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 672419373-(2-tert-butylphenyl)-1-(phenylsulfonyl)-1H-indole

생성물 1

HCID 672410893-(2-tert-butylphenyl)-1H-indole수율 26%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
100 °C

실험 절차

3-(2-tert-Butylphenyl)-1-(phenylsulfonyl)-1H-indole (172.6 mg, 0.443 mmol) was combined with tetrahydrofuran (2.0 mL) and 1 M tetrabutylammonium fluoride solution (2.21 mL) and heated to 100° C. for 20 minutes. The cooled reaction is charged to a silica gel column and purified by eluting with a gradient of ethyl acetate and hexanes to give 3-(2-tert-butylphenyl)-1H-indole (26.8 mg, 26%) as a colorless solid.

후처리

  1. customThe cooled reaction
  2. additionis charged to a silica gel column
  3. custompurified
  4. washby eluting with a gradient of ethyl acetate and hexanes

출처 및 근거

ORD 기록
ord-9477f39a4a7f45c9bc00c6c2ee272aaa
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07960569B2

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