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Imidazole → 3-(tert-Butyldimethylsilyloxy)pyrrolidin-2-one

HRID 2080688
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반응식

HRID 2080688 반응식
N1C=CN=C1.[C:6]([Si:10]([CH3:13])([CH3:12])Cl)([CH3:9])([CH3:8])[CH3:7].CN(C)C=O.[OH:19][CH:20]1[CH2:24][CH2:23][NH:22][C:21]1=[O:25]>O>[Si:10]([O:19][CH:20]1[CH2:24][CH2:23][NH:22][C:21]1=[O:25])([C:6]([CH3:9])([CH3:8])[CH3:7])([CH3:13])[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 795ImidazoleHCID 6228DimethylformamideHCID 28928tert-Butyldimethylsilyl chlorideHCID 102407723-Hydroxy-2-pyrrolidinone

생성물 1

HCID 146137613-(tert-Butyldimethylsilyloxy)pyrrolidin-2-one수율 11.4%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

In an ice bath, 300 mg of imidazole and 497 mg of tert-butyldimethylchlorosilane were added to a dimethylformamide (2 ml) solution of 255 mg of 3-hydroxypyrrolidin-2-one, and stirred for 1 hour. Water was added to the reaction liquid, extracted with ethyl acetate, and washed with hydrochloric acid (1 N) and saturated saline water. The organic layer was dried to obtain 370 mg of a crude product. 208 g of the product was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=9/1 to 2/8) to obtain 62 mg of the entitled compound as a white solid.

후처리

  1. extractionextracted with ethyl acetate
  2. washwashed with hydrochloric acid (1 N) and saturated saline water
  3. customThe organic layer was dried
  4. customto obtain 370 mg of a crude product
  5. custom208 g of the product was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=9/1 to 2/8)

출처 및 근거

ORD 기록
ord-f423ecac705f4a0a800404723fc9105e
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932394B2

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