反応 #75439

ord-553b75b593be4e02b96e885981ffd8c5

反応方程式

CC(C)CCON=O
isoamyl nitrite
COC(=O)CCC=C(C)C
methyl 5-methyl-4-hexenoate
Cl
HCl
COC(=O)CCC(N=O)C(C)(C)Cl
title product
COC(=O)CCC(N=O)C(C)(C)Cl
Methyl 5-chloro-4-nitroso-5-methylhexanoate

反応条件

温度
-15°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度maintaining the temperature of the reaction mixture below −5° C
  2. 2
    workup.ADDITIONAfter the addition
  3. 3
    ろ過filtered
  4. 4
    洗浄the precipitate washed with ethanol (−10° C.)
  5. 5
    その他The light blue colored solid thus obtained
  6. 6
    温度cooled to ˜−50° C.
  7. 7
    ろ過filtered

実験手順

A mixture of isoamyl nitrite (12 mL) and methyl 5-methyl-4-hexenoate (4.90 g, 35.00 mmol) was cooled to −15° C. To this stirred solution, concentrated HCl (12.5 mL) was added dropwise from an addition flask maintaining the temperature of the reaction mixture below −5° C. After the addition, the reaction mixture was stirred at 0° C. for 30 minutes, filtered and the precipitate washed with ethanol (−10° C.). The light blue colored solid thus obtained was dispersed in petroleum ether (50 mL), cooled to ˜−50° C. and filtered to provide the title product as a colorless solid. Yield: 3.0 g (41.3%); m.p. 90-91° C. 1H NMR (CDCl3) δ1.68 & 1.71[2s, 6H, C(CH3)2], 2.35[m, 4H, (CH2)2], 3.73(s, 3H, COOCH3) and 5.11(t, 1H, CH). MS m/e 208 (M+H)+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06699458B2uspto-grants-2004_03