تفاعل #1973909

ord-b7bd56265ca94cee90ebcded04ec4a78

معادلة التفاعل

CCOC(=O)C1CCCCC1=O
Ethyl 2-oxocyclohexanecarboxylate
BrBr
Bromine
CCOC(=O)C1=C(O)C(Br)CCC1
3-Bromo-2-hydroxy-1-enecarboxylic
المردود 94.4%
CCOC(=O)C1=C(O)C(Br)CCC1
3-Bromo-2-hydroxy-cyclohex-1-enecarboxylic acid ethyl ester
المردود 94.4%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm to RT over 90 min
  2. 2
    استخلاصextracted with ethyl acetate (3×200 mL)
  3. 3
    تجفيفThe combined organic layers were dried over magnesium sulfate
  4. 4
    ترشيحfiltered
  5. 5
    تركيزconcentrated in vacuo
  6. 6
    أخرىdried on the vacuum line for 18 h

الإجراء التجريبي

Ethyl 2-oxocyclohexanecarboxylate (30 g, 176 mmol, 28 mL) was dissolved in diethyl ether (30 mL) and cooled to 0° C. under nitrogen. Bromine (28 g, 176 mmol, 9.0 mL) was added dropwise over 15 min and the reaction mixture was allowed to warm to RT over 90 min. The mixture was slowly poured into ice-cold saturated aqueous potassium carbonate (250 mL) and extracted with ethyl acetate (3×200 mL). The combined organic layers were dried over magnesium sulfate, filtered, concentrated in vacuo and dried on the vacuum line for 18 h to afford 41.4 g (94%) of 3-Bromo-2-hydroxy-1-enecarboxylic acid ethyl ester (4) as a yellow oil. The structure was confirmed by 13C NMR (75 MHz, CDCl3): δC 14.1, 17.7, 21.8, 32.0, 60.0, 60.8, 99.7, 166.3, and 172.8.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08501153B2uspto-grants-2013_08