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Benzylamine → 2-benzylamino-N-(1,1-dimethylhexyl)acetamide

HRID 1277489
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반응식

HRID 1277489 반응식
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[CH2:10][C:11]([NH:13][C:14]([CH3:21])([CH3:20])[CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[O:12]>C1C=CC=CC=1>[CH2:1]([NH:8][CH2:10][C:11]([NH:13][C:14]([CH3:20])([CH3:21])[CH2:15][CH2:16][CH2:17][CH2:18][CH3:19])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7504BenzylamineHCID 234541292-chloro-N-(1,1-dimethylhexyl)acetamide

생성물 1

HCID 234541542-benzylamino-N-(1,1-dimethylhexyl)acetamide

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A solution of benzylamine (21.4 g, 0.2 mol) and 2-chloro-N-(1,1-dimethylhexyl)acetamide (20.6 g, 0.1 mol) in benzene (100 ml) was held at room temperature for five days then refluxed for 24 hours.The mixture was filtered and the filtrate was evaporated then distilled under reduced pressure to give 2-benzylamino-N-(1,1-dimethylhexyl)acetamide as a pale yellow oil, b.p. 153°-156° C. at 0.05 mm Hg.

후처리

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temperature
then refluxed for 24 hours
  • filtrationThe mixture was filtered
  • customthe filtrate was evaporated
  • distillationthen distilled under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-2c127f21a5014dcbba187fdf4486f427
    출처 데이터셋
    uspto-grants-1981_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04277498

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