تفاعل #1290

ord-d269152a14054777a8d6f6accb67dec8

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was refluxed (oil bath, 95°-100° C.) for 14 hours
  2. 2
    درجة الحرارةAfter refluxing for an additional 8 hours
  3. 3
    درجة الحرارةto reflux for another 14 hours (total 36 hours)
  4. 4
    ترشيحthe reaction mixture was filtered
  5. 5
    غسيلthe 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
    غسيلwashed with saturated sodium bicarbonate, water, brine
  8. 8
    تجفيفdried (sodium sulfate)
  9. 9
    ترشيحfiltered
  10. 10
    تركيزThe filtrate was concentrated in vacuo
  11. 11
    أخرىto afford 19.38 g
  12. 12
    أخرىof crude product as a yellow syrup which was used for the next reaction without purification

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723457uspto-grants-1998_03