反応 #1424

ord-a1ba75f5f74140a4b9b975cdffd4a9e5

反応方程式

CCN(CC)CC
triethylamine
CCN(CC)CC
triethylamine
CCOC(=O)CBr
ethyl bromoacetate
CCN(CC)CC
Triethylamine
CC(C)(C)OC(=O)NN
hydrazine carboxylic acid, 1,1-dimethylethyl ester
CCOC(=O)CBr
ethyl bromoacetate
CCOC(=O)CBr
ethyl bromoacetate
CCOC(=O)CNNC(=O)OC(C)(C)C
[2-[(1,1-dimethylethoxy)carbonyl]hydrazino]acetic acid, ethyl ester

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was refluxed (oil bath, 95°-100° C.) for 14 hours
  2. 2
    温度After refluxing for an additional 8 hours
  3. 3
    温度to reflux for another 14 hours (total 36 hours)
  4. 4
    ろ過the reaction mixture was filtered
  5. 5
    洗浄the solid triethylamine, hydrochloride salt was washed with ethyl acetate/hexane (1:1)
  6. 6
    workup.ADDITIONThe combined filtrate was diluted with ethyl acetate
  7. 7
    洗浄washed with saturated sodium bicarbonate, water, brine
  8. 8
    乾燥dried (sodium sulfate)
  9. 9
    ろ過filtered
  10. 10
    濃縮The filtrate was concentrated in vacuo
  11. 11
    その他to afford 19.38 g
  12. 12
    その他of crude product as a yellow syrup which was used for the next reaction without purification

実験手順

Triethylamine (13.94 ml., 0.1 mol.) was added to a solution of hydrazine carboxylic acid, 1,1-dimethylethyl ester (13.216 g., 0.1 mole) in benzene (100 ml.), followed by the addition of ethyl bromoacetate (11.09 ml., 0.1 mol.). The reaction mixture was refluxed (oil bath, 95°-100° C.) for 14 hours, after which triethylamine (1.4 ml., 0.01 mol.) was added followed by ethyl bromoacetate (1.1 ml., 0.01 mole). After refluxing for an additional 8 hours, triethylamine (2 ml., 0.015 mol.) and ethyl bromoacetate (1.4 ml., 0.013 mole) were added. The mixture was allowed to reflux for another 14 hours (total 36 hours). After cooling to room temperature, the reaction mixture was filtered and the solid triethylamine, hydrochloride salt was washed with ethyl acetate/hexane (1:1). The combined filtrate was diluted with ethyl acetate, washed with saturated sodium bicarbonate, water, brine, dried (sodium sulfate) and filtered. The filtrate was concentrated in vacuo to afford 19.38 g. of crude product as a yellow syrup which was used for the next reaction without purification.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723602uspto-grants-1998_03