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Methyl acetoacetate → Lauryl acetoacetate

HRID 1706845
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HRID 1706845 반응식
[C:1]([O:7][CH3:8])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].[CH2:9](O)[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]C>CO>[C:1]([O:7][CH2:8][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH3:9])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4]
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참가 물질

4

반응물 2

HCID 7757Methyl acetoacetateHCID 81931-Dodecanol

생성물 1

HCID 104190Lauryl acetoacetate

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
165 °C

실험 절차

Introduced into a reactor equipped with a stirrer mechanism, a Vigreux column with a column head and a reflux condenser are 464 g (4 moles) of methyl acetoacetate and 186 g of dodecyl alcohol. The temperature of the reaction medium is progressively raised to 165° C. and the methanol having formed is distilled until the reaction is terminated, that is to say, for about 8 hours. The methyl acetoacetate excess is eliminated under a reduced pressure of 8 mm Hg and the crude dodecyl acetoacetate is recovered, and this will be used as such for the preparation of the corresponding dihydropyridine derivative (Example 3).

후처리

  1. additionIntroduced into a reactor
  2. customequipped with a stirrer mechanism
  3. distillationis distilled until the reaction
  4. customis terminated
  5. customthe crude dodecyl acetoacetate is recovered
  6. customsuch for the preparation of the corresponding dihydropyridine derivative (Example 3)

출처 및 근거

ORD 기록
ord-91e3d53bae9d44b983700b368c80f3d0
출처 데이터셋
uspto-grants-1980_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04209439

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