1-Bromopentane → 2-Pentylbutanedioic acid

HRID 622337노트

반응식

HRID 622337 반응식
C([C:3]([CH2:16][CH3:17])([C:13]([O-:15])=[O:14])[C:4](CC)([C:8]([O-:10])=[O:9])C([O-])=O)C.[CH2:18](Br)[CH2:19][CH2:20]CC>>[CH2:16]([CH:3]([CH2:4][C:8]([OH:10])=[O:9])[C:13]([OH:15])=[O:14])[CH2:17][CH2:18][CH2:19][CH3:20]

참가 물질

3

반응물 2

HCID 80571-BromopentaneHCID 45790110HCID 45790110, 화합물

생성물 1

HCID 32796592-Pentylbutanedioic acid수율 153%

실험 절차

A method similar to that described by Devlin, et al, J. Chem. Soc., Perkin Transactions I, page 830 (1975) was used. Sodium ethoxide was formed by the addition of sodium metal (2.25 g, 91.59 mmol) to anhydrous EtOH (150 ml) under an N2 atmosphere. To the resultant solution was added triethyl-1,1,2-ethanetricaboxylate (obtained from Aldrich; 21 ml, 91.59 mmol) followed by dropwise addition of n-pentyl bromide (11.4 ml, 91.59 mmol). The mixture was brought to reflux and stirred overnight (19 hr). After the reaction had cooled, it was filtered and concentrated. The residue was treated with H2O and extracted with Et2O (three times). The combined organic extracts were dried (MgSO4), concentrated and purified by vacuum distillation (85° C./22.66 Pascals) to yield a colorless liquid (26.37 g, 91% yield).

후처리

  1. temperatureto reflux
  2. temperatureAfter the reaction had cooled
  3. filtrationit was filtered
  4. concentrationconcentrated
  5. additionThe residue was treated with H2O
  6. extractionextracted with Et2O (three times)
  7. dry with materialThe combined organic extracts were dried (MgSO4)
  8. concentrationconcentrated
  9. distillationpurified by vacuum distillation (85° C./22.66 Pascals)

출처 및 근거

ORD 기록
ord-180871fc63bd4614bfb8e79ede8ecf13
출처 데이터셋
uspto-grants-1988_09
특허 번호
US04771038

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