تفاعل #95933

ord-26d3bd2635924f5d8c9669e11ae3ebee

معادلة التفاعل

CO
methanol
CC(C)(C)OC(=O)CCCCCCBr
7-bromoheptanoic acid t-butyl ester
[H-]
hydride
O
water
O=CCCCCCCBr
title compound
المردود 85.3%
O=CCCCCCCBr
7-bromoheptanaldehyde
المردود 85.3%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred at 30° C. to 40° C. for 1 hour
  2. 2
    ترشيحThe deposited crystals were filtered out
  3. 3
    تركيزthe filtrate was concentrated under reduced pressure
  4. 4
    أخرىThe residue was purified by column chromatography on silica gel using
  5. 5
    workup.ADDITIONa mixture of methylene and chloride and cyclohexane (1:1) as an eluent

الإجراء التجريبي

To 8.5 g of 7-bromoheptanoic acid t-butyl ester (prepared as described in Reference Example 1) in 80 ml of methylene chloride was added dropwise 18.2 ml of a 25% solution of diisobutyl alminium hydride in toluene at -78° C. over a period of 1 hours. The solution was stirred at the same temperature, to which was added 5 ml of methanol at from 0° C. to 10° C. and then added 10 ml of water, and the mixture was stirred at 30° C. to 40° C. for 1 hour. The deposited crystals were filtered out, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of methylene and chloride and cyclohexane (1:1) as an eluent to give 5.28 g of the title compound having the following physical characteristic:

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04346099uspto-grants-1982_08