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Ethyl oxoacetate → Ethyl 2-((tert-butylsulfinyl)imino)acetate

HRID 594406
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HRID 594406 반응식
O=[CH:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[CH3:8][C:9]([S:12]([NH2:14])=[O:13])([CH3:11])[CH3:10]>C(Cl)Cl>[C:9]([S:12]([N:14]=[CH:2][C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:13])([CH3:11])([CH3:10])[CH3:8]
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참가 물질

4

반응물 2

HCID 70211Ethyl oxoacetateHCID 3382465Tert-Butanesulfinamide

생성물 1

HCID 72998703Ethyl 2-((tert-butylsulfinyl)imino)acetate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of ethyl 2-oxoacetate (50% solution in toluene; 4.066 g; 20.00 mmol), 2-methylpropane-2-sulfinamide (2.424 g; 20.00 mmol), and 4 angstrom molecular sieves (60 g) in anh. DCM (250 ml) was stirred at rt, under nitrogen, for 65 h. The reaction mixture was then filtered over celite, and the separated solids were washed with AcOEt (3×200 ml). The filtrate was then dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording ethyl 2-((tert-butylsulfinyl)imino)acetate as a yellow oil.

후처리

  1. filtrationThe reaction mixture was then filtered over celite
  2. washthe separated solids were washed with AcOEt (3×200 ml)
  3. dry with materialThe filtrate was then dried over anh. MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-b9eaeb5e5f914fa5b1bf67f151028b12
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242970B2

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