تفاعل #927244

ord-01faa00a5ee743848313ef65f3dfd14c

معادلة التفاعل

CCCCCC
Hexane
O
water
BrCCCCCCBr
1,6-dibromohexane
C[O-].[Na+]
sodium methoxide
BrCCCCCCBr
1,6-dibromohexane
C[O-].[Na+]
sodium methoxide
COCCCCCCBr
6-bromohexyl methyl ether
المردود 93.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITthe reaction mixture was held an additional hour
  2. 2
    غسيلthe organic phase was washed with brine
  3. 3
    تجفيفdried with magnesium sulfate
  4. 4
    ترشيحfiltered
  5. 5
    workup.DISTILLATIONFractional distillation under vacuum

الإجراء التجريبي

6-Bromohexyl methyl ether was prepared from 1,6-dibromohexane. To 48.8 g (200 mmol) of 1,6-dibromohexane at 60° C. was added 44 g (200 mmol) of a 25% solution of sodium methoxide in methanol. The reaction mixture was held 0.5 hours, then an additional 4 g of sodium methoxide solution was added, and the reaction mixture was held an additional hour. Hexane and water were added, the organic phase was washed with brine and dried with magnesium sulfate, filtered and stripped. Fractional distillation under vacuum gave 93% pure 6-bromohexyl methyl ether. This bromide was converted to the Grignard reagent, which was converted to 1-(7-methoxyheptyl)-cyclopropene in the same manner that pentylmagnesium bromide was converted to 1-hexylcyclopropene.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06365549B2uspto-grants-2002_04