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3-Amino-1-propanol → N-(3-Hydroxypropyl)trifluoroacetamide

HRID 1484479
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HRID 1484479 반응식
[F:1][C:2]([F:9])([F:8])[C:3]([O:5]CC)=O.[NH2:10][CH2:11][CH2:12][CH2:13][OH:14].C1C=C2C(C(O)(O)C(=O)C2=CC=1)=O>>[OH:14][CH2:13][CH2:12][CH2:11][NH:10][C:3](=[O:5])[C:2]([F:1])([F:8])[F:9]
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참가 물질

4

반응물 3

HCID 90863-Amino-1-propanolHCID 9794Ethyl trifluoroacetateHCID 10236Ninhydrin

생성물 1

HCID 1987732N-(3-Hydroxypropyl)trifluoroacetamide

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온도
0 °C

실험 절차

Ethyl trifluoroacetate (14.1 g; 0.1 mol) was added dropwise to 3-amino-1-propanol (6 g; 0.08 mol) cooled to 0° C. The mixture was stirred at 0° C. for 60 min; the completion of the reaction was confirmed by a negative Ninhydrin test. Volatiles were removed by rotary evaporation and the residue purified by vacuum distillation to provide N-(3-hydroxypropyl)trifluoroacetamide as a clear, viscous liquid in a yield of 13.4 g (98%). 1H-NMR (500 MHz, CDCl3): δ=3.52-3.57 ppm (m, 2H), 2.17 ppm (bs, 1H), 3.54 ppm (dt, J=6.0, 6.0 Hz, 2H), 3.81 ppm (t, J=5.5 Hz, 2H), 7.28 ppm (bs, 1H), 13C-NMR (500 MHz, CDCl3): δ=30.42, 38.35, 61.05, 115.93 ppm (q, J=1142 Hz), 157.76 ppm (q, J=150 Hz).

후처리

  1. customVolatiles were removed by rotary evaporation
  2. distillationthe residue purified by vacuum distillation

출처 및 근거

ORD 기록
ord-4cd858982cf945d8925dcb0dd5c6d2d5
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09422232B2

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