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Ammonia → HCID 131718530, 화합물

HRID 1728460
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HRID 1728460 반응식
[C:1]([O:11][C:12]([C:18]([O:21][C:22]([C:31](F)=[O:32])([C:27]([F:30])([F:29])[F:28])[C:23]([F:26])([F:25])[F:24])([F:20])[F:19])([C:14]([F:17])([F:16])[F:15])[F:13])([C:4]([C:7]([F:10])([F:9])[F:8])([F:6])[F:5])([F:3])[F:2].[NH3:34]>>[C:1]([O:11][C:12]([C:18]([O:21][C:22]([C:31]([NH2:34])=[O:32])([C:27]([F:30])([F:29])[F:28])[C:23]([F:26])([F:25])[F:24])([F:20])[F:19])([C:14]([F:17])([F:16])[F:15])[F:13])([C:4]([C:7]([F:10])([F:9])[F:8])([F:6])[F:5])([F:3])[F:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 222AmmoniaHCID 131718529HCID 131718529, 화합물

생성물 1

HCID 131718530HCID 131718530, 화합물수율 86%

실험 절차

The acid fluoride, C3F7OCF(CF3)CF2OC(CF3)2COF, (4.51 g, 8.20 mmol) was reacted with ammonia (18.88 mmol) in vacuo at -78° C. for 10 minutes, then at -23° C. for 3 hours. The volatiles were removed at room temperature by pumping and the involatile residue was treated with dry Freon 113 (20 ml) and filtered in an inert atmosphere enclosure. The filtrate, after Freon 113 removal, gave 3.82 g (86% yeild) of C3F7OCF(CF3)CF2OC(CF3)2CONH2 which was characterized by mass spectrometry. MS(70 eV) m/e (intensity, ion): 526 (2.1%, M-F), 360 (29.4%, M-C3F7O), 260 (7.0%, CF2OC(CF3)2CONH2), 194 (17.2%, C(CF3), 169 (25.7%, C3F7), 69 (48.4%, CF3), 44 (100%, CONH2), 169 (25.7%, C3F7), 69 (48.4%, CF3), 44 (100%, CONH2).

후처리

  1. customThe volatiles were removed at room temperature
  2. addition
the involatile residue was treated
  • dry with materialwith dry Freon 113 (20 ml)
  • filtrationfiltered in an inert atmosphere enclosure
  • customThe filtrate, after Freon 113 removal
  • 출처 및 근거

    ORD 기록
    ord-62bdd87fb2474409b98b5cfa1ec9964a
    출처 데이터셋
    uspto-grants-1994_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05326910

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