تفاعل #1674562

ord-cd1b08a65d0046f98fa9e81b293c8e7e

معادلة التفاعل

Fc1cc(Br)cc(OCc2ccccc2)c1
3-benzyloxy-5-fluorobromobenzene
[Mg]
magnesium
COC1CCCC1=O
2-methoxycyclopentanone
Fc1cc(OCc2ccccc2)c[c]([Mg][Br])c1
3-benzyloxy-5-fluorophenylmagnesium bromide
COC1CCCC1(O)c1cc(F)cc(OCc2ccccc2)c1
1-(3-benzyloxy-5-fluorophenyl)-2-methoxycyclopentanol
المردود 62.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter repetition of the above reaction
  2. 2
    أخرىprepared
  3. 3
    درجة الحرارةby heating
  4. 4
    أخرىThe mixture was evaporated
  5. 5
    أخرىthe residue was partitioned between diethyl ether and water
  6. 6
    غسيلThe organic layer was washed with water
  7. 7
    تجفيفdried (MgSO4)
  8. 8
    أخرىevaporated
  9. 9
    أخرىThe residue was purified by column chromatography
  10. 10
    workup.ADDITIONa 9:1 v/v mixture of methylene chloride and diethyl ether as eluent

الإجراء التجريبي

After repetition of the above reaction, a solution of 2-methoxycyclopentanone (12.5 g) in tetrahydrofuran (10 ml) was added to a solution of 3-benzyloxy-5-fluorophenylmagnesium bromide [prepared by heating a mixture of 3-benzyloxy-5-fluorobromobenzene (31 g), magnesium powder (2.65 g) and tetrahydrofuran (20 ml) to 40° C. for 2 hours] and the mixture was stirred at ambient temperature for 2 hours. The mixture was evaporated and the residue was partitioned between diethyl ether and water. The organic layer was washed with water, dried (MgSO4) and evaporated. The residue was purified by column chromatography using a 9:1 v/v mixture of methylene chloride and diethyl ether as eluent. There was thus obtained, as a mixture of diastereoisomers, 1-(3-benzyloxy-5-fluorophenyl)-2-methoxycyclopentanol (21.7 g, 62%), as an oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05217977uspto-grants-1993_06