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Pyridine → 3-Phenylpropyl carbonochloridate

HRID 530470
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인쇄 미리보기

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HRID 530470 반응식
[Cl:1][C:2](Cl)([O:4]C(=O)OC(Cl)(Cl)Cl)Cl.N1C=CC=CC=1.[C:19]1([CH2:25][CH2:26][CH2:27][OH:28])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C1(C)C=CC=CC=1>[C:19]1([CH2:25][CH2:26][CH2:27][O:28][C:2]([Cl:1])=[O:4])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 31234BenzenepropanolHCID 94429Triphosgene

생성물 1

HCID 214186893-Phenylpropyl carbonochloridate수율 85%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
0 °C

실험 절차

In a four necked round bottom flask, triphosgene (5.45 g, 55.1 mmol) was dissolved in toluene (80 mL) under argon. After cooling at 0° C., pyridine (4.8 mL, 58.8 mmol) was added dropwise during 1 h and the resulting suspension stirred for further 1 h at 0° C. 3-phenyl-1-propanol (5 mL, 36.8 mmol) was added dropwise in 30 min. After stirring at rt for 24 h, the solid was filtered off and the solvent removed under vacuum, yielding the title compound (6.2 g, 85%) as pale yellow oil, which was used in the next step without further purification. FTIR (cm−1): 3086, 3065, 3027, 2995, 2932, 2862, 1776, 1743, 1603, 1496, 1454, 1262, 1148, 745, 699.

후처리

  1. stirringAfter stirring at rt for 24 h
  2. filtrationthe solid was filtered off
  3. customthe solvent removed under vacuum

출처 및 근거

ORD 기록
ord-831f1103789645beb64d32149917cc55
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353075B2

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