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Ethane, 2-bromo-1,1-diethoxy- → 4-(2,2-Diethoxyethylthiomethyl)pyridine

HRID 615593
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인쇄 미리보기

반응식

HRID 615593 반응식
C[O-].[Na+].[N:4]1[CH:9]=[CH:8][C:7]([CH2:10][SH:11])=[CH:6][CH:5]=1.[CH2:12]([O:14][CH:15]([O:18][CH2:19][CH3:20])[CH2:16]Br)[CH3:13]>C(O)C>[CH2:12]([O:14][CH:15]([O:18][CH2:19][CH3:20])[CH2:16][S:11][CH2:10][C:7]1[CH:8]=[CH:9][N:4]=[CH:5][CH:6]=1)[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 74852Ethane, 2-bromo-1,1-diethoxy-HCID 10942334Sodium MethoxideHCID 13092602Pyridin-4-ylmethanethiol

생성물 1

HCID 130926034-(2,2-Diethoxyethylthiomethyl)pyridine

시약·촉매·용매 1

HCID 702Ethanol용매3회

실험 절차

Under a nitrogen atmosphere, sodium methoxide (0.60 g., 11 moles) is dissolved in approximately 15 ml. of stirring ethanol and cooled in an ice bath. 4-Picolyl mercaptan (1.4 g., 11 mmoles) in approximately 3 ml. of absolute ethanol is added over 5 minutes and the mixture stirred for 15 minutes. Bromoacetaldehyde diethylacetal (2.4 g., 11 mmoles) in approximately 15 ml. of absolute ethanol is then added over 5 minutes. The reaction mixture is warmed to room temperature and stirred for 16 hours. The reaction mixture is filtered and the filtrate evaporated to yield title product, which if desired, can be further purified by chromatography on silica gel.

후처리

  1. stirringstirred for 16 hours
  2. filtrationThe reaction mixture is filtered
  3. customthe filtrate evaporated

출처 및 근거

ORD 기록
ord-caa855c264d64e71a12869e6c367f7c7
출처 데이터셋
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04500535

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