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Sodium Hydroxide → HCID 85809393, 화합물

HRID 2414999
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HRID 2414999 반응식
[CH2:1]([O:8][CH2:9][CH:10]([CH2:19][OH:20])[O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].[C:23]([O:27][C:28](=[O:31])[CH2:29]Br)([CH3:26])([CH3:25])[CH3:24]>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.C1(C)C=CC=CC=1>[C:23]([O:27][C:28](=[O:31])[CH2:29][O:20][CH2:19][CH:10]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH2:9][O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)([CH3:26])([CH3:25])[CH3:24]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 14798Sodium HydroxideHCID 79177tert-Butyl bromoacetateHCID 43908021,2-di-O-benzyl-glycerol

생성물 1

HCID 85809393HCID 85809393, 화합물

시약·촉매·용매 2

HCID 94433Tetrabutylammonium hydrogen sulfate촉매HCID 1140Toluene용매

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온도
0 °C

실험 절차

100 g (376.2 mmol) of 1,2-di-O-benzyl-glycerol [produced according to Chem. Phys. Lipids (1987), 43(2), 113-277] and 5 g of tetrabutylammonium hydrogen sulfate are dissolved in a mixture that consists of 400 ml of toluene and 200 ml of 50% aqueous sodium hydroxide solution. At 0° C., 78 g (400 mmol) of 2-bromoacetic acid-t butyl ester is added in drops over 30 minutes, and then it is stirred for 3 hours at 0° C. The organic phase is separated, dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: n-hexane/acetone=20:1).

후처리

  1. customThe organic phase is separated
  2. customdried on magnesium sulfate
  3. customevaporated to the dry state in a vacuum
  4. customThe residue is chromatographed on silica gel (mobile solvent: n-hexane/acetone=20:1)

출처 및 근거

ORD 기록
ord-ad49a539b6404895adaada7e54f5e627
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06818203B2

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