反応 #48033

ord-a821111b5cd14d5c9654f24ee869be1c

反応方程式

Nc1ccc(Cl)cc1
4-chloroaniline
O=N[O-].[Na+]
NaNO2
CC(=O)[O-].[Na+]
NaOAc
CCOC(=O)C(Cl)C(C)=O
ethyl 2-chloro-3-oxobutanoate
CCOC(=O)C(Cl)=NNc1ccc(Cl)cc1
ethyl 2-chloro[(4-chlorophenyl)hydrazono]acetate
収率 73.4%

反応条件

温度
2.5°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGAfter stirring the resulting mixture for 1 hour the formed precipitate
  2. 2
    ろ過is collected by filtration
  3. 3
    洗浄washed with ethanol
  4. 4
    その他dried in vacuo

実験手順

Part A: To a stirred solution of 4-chloroaniline (15.68 gram, 0.123 mol) in ice (30 ml) and concentrated hydrochloric acid (30 ml) is slowly added a solution of NaNO2 (9.0 gram, 0.13 mol) in water (16 ml) and the resulting solution is stirred for 1Hour at 0-5° C. and subsequently added to a cold mixture of NaOAc (32 gram, 0.39 mol), ethanol (520 ml) and ethyl 2-chloro-3-oxobutanoate (16.6 ml, 0.12 mol). After stirring the resulting mixture for 1 hour the formed precipitate is collected by filtration, washed with ethanol and dried in vacuo to give ethyl 2-chloro[(4-chlorophenyl)hydrazono]acetate (22.99 gram, 73% yield). Melting point: 147.5-149.5° C. 1H-NMR (200 MHz, CDCl3): 1.40 (t, J=7 Hz, 3H), 4.39 (q, J=7 Hz, 2H), 7.16 (br d, J=8 Hz, 2H), 7.30 (br d, J=8 Hz, 2H), 8.31 (br s, 1H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07745476B2uspto-grants-2010_06