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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Pyridine → 5-Oxo-2-pyrrolidine carboxylic acid n-dodecylamide

HRID 1605033
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반응식

HRID 1605033 반응식
[CH2:1]([NH2:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].N1C=CC=CC=1.[O:20]=[C:21]1[NH:25][CH:24]([C:26](Cl)=[O:27])[CH2:23][CH2:22]1>O>[CH2:1]([NH:13][C:26]([CH:24]1[CH2:23][CH2:22][C:21](=[O:20])[NH:25]1)=[O:27])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 13583DodecylamineHCID 123788552-Pyrrolidinecarbonyl chloride, 5-oxo-

생성물 1

HCID 542276525-Oxo-2-pyrrolidine carboxylic acid n-dodecylamide

시약·촉매·용매 1

HCID 962Water용매

실험 절차

While cooling and stirring a mixture consisting of 9.2 gm (0.05 mol) of n-dodecylamine and 50 ml of pyridine, 17.3 gm (0.05 mol) of 5-oxo-2-pyrrolidine carboxylic acid chloride were added thereto in small portions, and the resulting mixture was stirred for one hour at room temperature. Thereafter, the reaction mixture was admixed with water, acidified and extracted with chloroform. The organic phase was separated, washed with water, dried and evaporated. The residue was recrystallized from ethyl acetate, yielding 9.0 gm (62% of theory) of the compound of the formula ##EQU5## which had a melting point of 114°-116°C.

후처리

  1. temperatureWhile cooling
  2. additionwere added
  3. stirringin small portions, and the resulting mixture was stirred for one hour at room temperature
  4. extractionextracted with chloroform
  5. customThe organic phase was separated
  6. washwashed with water
  7. customdried
  8. customevaporated
  9. customThe residue was recrystallized from ethyl acetate
  10. customyielding 9.0 gm (62% of theory) of the compound of the formula ##EQU5## which

출처 및 근거

ORD 기록
ord-6941d11eada34d89840948d315ea7f87
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03948943

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