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Chlorosuccinimide → HCID 46218813, 화합물

HRID 386849
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HRID 386849 반응식
[Cl:1]N1C(=O)CCC1=O.[O:9]1[CH2:14][CH2:13][CH:12]([C:15]2[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][C:16]=2[OH:22])[CH2:11][CH2:10]1>ClCCl>[Cl:1][C:19]1[CH:20]=[C:15]([CH:12]2[CH2:11][CH2:10][O:9][CH2:14][CH2:13]2)[C:16]([OH:22])=[CH:17][C:18]=1[OH:21]
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 462078334-(tetrahydro-2H-pyran-4-yl)-1,3-benzenediol

생성물 1

HCID 46218813HCID 46218813, 화합물수율 17%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

2.4 g of N-chlorosuccinimide are added to a solution of 2 g of 4-(tetrahydropyran-4-yl)benzene-1,3-diol (Example 1) in 30 ml of dichloromethane at 0° C. The reaction mixture is stirred at ambient temperature for 16 hours. The reaction mixture is extracted with dichloromethane and then washed with water. The organic phases are combined and then dried over sodium sulphate. The residue is chromatographed on silica gel (75/25 heptane/ethyl acetate). 400 mg of 4-chloro-6-(tetrahydropyran-4-yl)benzene-1,3-diol are obtained. Yield=17%.

후처리

  1. extractionThe reaction mixture is extracted with dichloromethane
  2. washwashed with water
  3. dry with materialdried over sodium sulphate
  4. customThe residue is chromatographed on silica gel (75/25 heptane/ethyl acetate)

출처 및 근거

ORD 기록
ord-927ece7fa95d4b21af35b319ba63e514
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08372879B2

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