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Hydrazine hydrate (1:1) → [2-(2-Methoxyethoxy)-ethyl]-hydrazine

HRID 12901
ノート
印刷プレビュー

反応式

HRID 12901 の反応式
O.[NH2:2][NH2:3].Br[CH2:5][CH2:6][O:7][CH2:8][CH2:9][O:10][CH3:11]>C(O)C>[CH3:11][O:10][CH2:9][CH2:8][O:7][CH2:6][CH2:5][NH:2][NH2:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 1235321-Bromo-3,6-dioxaheptane

生成物 1

HCID 18959038[2-(2-Methoxyethoxy)-ethyl]-hydrazine収率 85%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of hydrazine monohydrate (44.0 mL, 1.00 mol) in ethanol (75 mL) at 0° C. in an ice-water bath was added 1-(2-bromoethoxy)-2-methoxyethane (13.6 mL, 0.100 mol) drop-wise over 20 minutes. The reaction was then allowed to warm to room temperature and stir for 5 minutes and then heated to 40° C. in a preheated oil bath for 12 hours. The reaction was then cooled to room temperature and concentrated to remove the ethanol. The remaining aqueous layer was extracted with methylene chloride (2×100 mL) and diethyl ether (2×100 mL). The organic layers were combined and dried over anhydrous Na2SO4, filtered and concentrated to provide [2-(2-methoxyethoxy)-ethyl]-hydrazine as a light yellow oil (10.29 g, 85%).

後処理

  1. temperatureheated to 40° C. in a preheated oil bath for 12 hours
  2. temperatureThe reaction was then cooled to room temperature
  3. concentrationconcentrated
  4. customto remove the ethanol
  5. extractionThe remaining aqueous layer was extracted with methylene chloride (2×100 mL) and diethyl ether (2×100 mL)
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-1759ce57e6de40e986407126f2e925cc
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07728029B2

反応ノート

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