تفاعل #742287

ord-6a371eaa1e7b4502a8e881f0bc8a28c2

معادلة التفاعل

CC1C(=O)CC2(C)CCC1C2
1,4-Dimethyl-bicyclo[3.2.1]octan-3-one
[BH4-].[Na+]
NaBH4
CC1C(O)CC2(C)CCC1C2
1,4-dimethyl-bicyclo[3.2.1]octan-3-ol
المردود 95.2%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةrefluxed for 30 minutes
  2. 2
    أخرىquenched with acetone
  3. 3
    أخرىThe organic layer was separated
  4. 4
    تركيزconcentrated

الإجراء التجريبي

1,4-Dimethyl-bicyclo[3.2.1]octan-3-one (160 g, 1.05 mol, obtained as above in EXAMPLE III) was added to a NaBH4 suspension (12 g, 0.33 mol) in isopropanol (200 mL), and refluxed for 30 minutes. The reaction mixture was cooled to room temperature, and quenched with acetone followed by acetic acid. The organic layer was separated and concentrated to provide crude 1,4-dimethyl-bicyclo[3.2.1]octan-3-ol (150 g, 1.0 mol), which was then added to dimethyl carbonate (CO(OCH3)2, 270 g, 3 mol), and potassium tert-butoxide ((CH3)3COK, 25 g), and refluxed for 3 hours. The volatile ingredients were removed with a Dean Stark trap. The reaction mixture was subsequently quenched with acetic acid, and washed with water. Fractional distillation of the organic layer provided carbonic acid 1,4-dimethyl-bicyclo[3.2.1]oct-3-yl ester methyl ester (125 g) having a boiling point of 65° C. at a pressure of 0.5 mmHg

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08071529B1uspto-grants-2011_12