تفاعل #632003

ord-5bd555d0153649c4b0334bc3927ea25f

معادلة التفاعل

CCC1CC1(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
product
CCC1CC1(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
2-ethylcyclopropane-1,1-dicarboxylic acid di-tert-butyl ester
CC(C)(C)[O-].[K+]
potassium tert-butoxide
CCC1CC1(C(=O)O)C(=O)OC(C)(C)C
desired product
المردود 69.0%
CCC1CC1(C(=O)O)C(=O)OC(C)(C)C
racemic 2-Ethylcyclopropane-1,1-dicarboxylic acid tert-butyl ester
المردود 69.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed with diethyl ether (3×)
  2. 2
    أخرىwas adjusted to acidic pH with a 10% aqueous citric acid solution at 0° C.
  3. 3
    استخلاصextracted with ethyl acetate (3×)
  4. 4
    غسيلThe combined organic layers were washed with water (2×), brine
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated in vacuo

الإجراء التجريبي

The product of Step 1 (18.3 g, 67.8 mmol) was added to a suspension of potassium tert-butoxide (33.55 g, 299.0 mmol) in dry diethyl ether (500 mL) at 0° C., treated with H2O (1.35 mL, 75.0 mmol), and was vigorously stirred overnight at room temperature. The reaction mixture was poured in a mixture of ice and water and washed with diethyl ether (3×). The aqueous layer was adjusted to acidic pH with a 10% aqueous citric acid solution at 0° C. and extracted with ethyl acetate (3×). The combined organic layers were washed with water (2×), brine, dried (MgSO4), filtered, and concentrated in vacuo to provide the desired product as a pale yellow oil (10 g, 46.8 mmol, 69% yield).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07935670B2uspto-grants-2011_05