반응 #41184

ord-25c3b70965af461399f9fca20de6164c

반응 방정식

CC(C)(C)OC(=O)NN
hydrazinecarboxylic acid tert-butyl ester
Cc1ccccc1
toluene
[K+].[OH-]
potassium hydroxide
COCCCBr
1-bromo-3-methoxypropane
COCCCN(N=C(C)C)C(=O)OC(C)(C)C
N′-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester
수율 98.0%

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The solution was then heated to 80° C. for 3 h
  2. 2
    온도The solution was cooled to room temperature
  3. 3
    세척washed with water (3×150 mL) until the water layer
  4. 4
    건조The organic layer was dried over anhydrous magnesium sulfate
  5. 5
    여과filtered
  6. 6
    농축concentrated in vacuo

실험 절차

To a solution of hydrazinecarboxylic acid tert-butyl ester (4.67 g, 27.16 mmol) in toluene (90 mL) was added pulverized potassium hydroxide (1.98 g, 35.3 mmol) and tetrabutylammonium hydrogensulfate (904 mg, 2.72 mmol). The solution was heated to 50° C. in a preheated oil bath and 1-bromo-3-methoxypropane (3.67 mL, 32.6 mmol) was added drop-wise over 45 minutes. The solution was then heated to 80° C. for 3 h. The solution was cooled to room temperature and washed with water (3×150 mL) until the water layer was neutral. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to provide N′-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester as a viscous oil (6.49 g, 98%), which was used without further purification. Mass spectrum: m/z: 245.4 (M+1).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07728029B2uspto-grants-2010_06