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Butyryl chloride → HCID 70511397, 화합물

HRID 1632316
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HRID 1632316 반응식
Cl.[CH:2]([S:5][C:6]1[CH:11]=[CH:10][C:9]([CH:12]([OH:24])[CH:13]([NH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[CH3:14])=[CH:8][CH:7]=1)([CH3:4])[CH3:3].[C:25]([Cl:30])(=[O:29])[CH2:26][CH2:27][CH3:28]>C(#N)C>[ClH:30].[C:25]([O:24][CH:12]([C:9]1[CH:10]=[CH:11][C:6]([S:5][CH:2]([CH3:4])[CH3:3])=[CH:7][CH:8]=1)[CH:13]([NH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[CH3:14])(=[O:29])[CH2:26][CH2:27][CH3:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8855Butyryl chlorideHCID 30169124-(Isopropylthio)-alpha-(1-(octylamino)ethyl)benzyl alcohol hydrochloride

생성물 1

HCID 70511397HCID 70511397, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

A mixture made of 10 gr (27 mmol) of 1-(4-isopropylthiophenyl)-2-n-octylamino-1-propanol hydrochloride and 11.4 gr (107 mmol) of butyryl chloride is heated at reflux temperature until a limpid solution is obtained. 10 ml of acetonitrile are added and reflux is maintained for about 2 hours. The solution so obtained is diluted with 40 ml of acetonitrile before being cooled. The white solid if filtered off. After recrystallisation from acetonitrile, the product weights 6.4 gr (14 mmol, 52%) and has a melting point of 104.1° C.

후처리

  1. temperatureis heated
  2. temperatureat reflux temperature until a limpid solution
  3. customis obtained
  4. temperaturereflux
  5. temperatureis maintained for about 2 hours
  6. customThe solution so obtained
  7. temperaturebefore being cooled
  8. filtrationThe white solid if filtered off
  9. customAfter recrystallisation from acetonitrile

출처 및 근거

ORD 기록
ord-06ce6b5f8bc74c7d87b645015ce42fce
출처 데이터셋
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04474977

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