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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl isothiocyanate → HCID 21519704, 화합물

HRID 1283267
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HRID 1283267 반응식
[C:1]([C:5]1[CH2:6][CH2:7][NH:8][CH2:9][CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:11]([N:13]=[C:14]=[S:15])[CH3:12]>O1CCCC1>[CH2:11]([NH:13][C:14]([N:8]1[CH2:7][CH:6]=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[CH2:10][CH2:9]1)=[S:15])[CH3:12]
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참가 물질

4

반응물 2

HCID 10966Ethyl isothiocyanateHCID 215197034-tert-Butyl-1,2,3,6-tetrahydropyridine

생성물 1

HCID 21519704HCID 21519704, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

In 20 ml. of anhydrous tetrahydrofuran there is dissolved 5.0 grams of 4-t-butyl-1,2,3,6-tetrahydropyridine. Stirring is initiated and there is added 3.14 grams of ethylisothiocyanate in 10 ml. of anhydrous tetrahydrofuran allowing the reaction to run at room temperature. After stirring the reaction mixture for 18 hours, the tetrahydrofuran is evaporated in vacuo to give N-ethyl-4-t-butyl-1,2,3,6-tetrahydro-1-pyridinethiocarboxamide.

후처리

  1. customto run at room temperature
  2. stirringAfter stirring the reaction mixture for 18 hours
  3. customthe tetrahydrofuran is evaporated in vacuo

출처 및 근거

ORD 기록
ord-ad7a2e1bbe2747feab55afc80d6d5c0b
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03974283

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