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Diethyl Ether → 2-(3,5-Dichlorophenoxy)ethylamine

HRID 480312
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HRID 480312 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:19]=[C:20]([Cl:22])[CH:21]=1)[O:5][CH2:6][CH2:7][N:8]1C(=O)C2C(=CC=CC=2)C1=O.O.NN.CCOCC.[OH-].[K+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([CH:19]=[C:20]([Cl:22])[CH:21]=1)[O:5][CH2:6][CH2:7][NH2:8]
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참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 14797Potassium HydroxideHCID 24654Hydrazine hydrate (1:1)HCID 7571580HCID 7571580, 화합물

생성물 1

HCID 499912-(3,5-Dichlorophenoxy)ethylamine수율 109.9%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 2-[2-(3,5-dichloro-phenoxy)-ethyl]-isoindole-1,3-dione (1.29 g, 3.84 mmol) and hydrazine hydrate (202 mg, 4.05 mmol) in MeOH (16 mL) was heated at reflux for 2 h. The mixture was cooled to room temperature and Et2O was added. The suspension was shaken with 40% aqueous potassium hydroxide. The aqueous solution was extracted with Et2O (3×) and the combined organic layers were dried (K2CO3), filtered, and concentrated to provide the title compound (870 mg). 1HNMR (400 MHz, CDCl3) δ 6.95 (m, 1H), 6.80 (m, 2H), 3.95 (m, 2H), 3.07 (t, 2H), 1.70 (bs, 2H).

후처리

  1. temperatureat reflux for 2 h
  2. extractionThe aqueous solution was extracted with Et2O (3×)
  3. dry with materialthe combined organic layers were dried (K2CO3)
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-04cdd80d0b624e71b918e27c2f4cf126
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06649657B2

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