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2-Methyl-2-pentenal → 4-Methylhept-4-en-1-yn-3-ol

HRID 1111684
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HRID 1111684 반응식
[C:1]([Mg]Br)#[CH:2].[CH3:5][C:6](=[CH:9][CH2:10][CH3:11])[CH:7]=[O:8].[Cl-].[NH4+]>O1CCCC1>[C:1]([CH:7]([OH:8])[C:6]([CH3:5])=[CH:9][CH2:10][CH3:11])#[CH:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 121772-Methyl-2-pentenalHCID 25517Ammonium ChlorideHCID 178418486HCID 178418486, 화합물

생성물 1

HCID 537300694-Methylhept-4-en-1-yn-3-ol수율 364.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of ethynyl magnesium bromide (prepared from 2.91 g of magnesium) in 100 ml of tetrahydrofuran, was added dropwise 9.8 g of 2-methyl-2-pentenal at a temperature from 0° C to 10° C under cooling with ice-bath. The resulting reaction solution was stirred for 3 hours at room temperature to complete the reaction and then the reaction solution was poured into a saturated ammonium cloride solution with 50 g of ice. After stirring, the solution was extracted twice with 100 ml of ether and the organic layers were combined, and then washed with 50 ml of a saturated sodium chloride solution. After the organic layer had been dried over anhydrous sodium sulfate, the ether was evaporated. The remaining liquid was purified by distillation at reduced pressure to obtain 10.2 g of a colorless oily 1-ethynyl-2-methyl-2-pentenyl alcohol, b.p. 85°-88° C/20 mmHg.

후처리

  1. temperatureunder cooling with ice-bath
  2. customThe resulting reaction solution
  3. customthe reaction
  4. stirringAfter stirring
  5. extractionthe solution was extracted twice with 100 ml of ether
  6. washwashed with 50 ml of a saturated sodium chloride solution
  7. dry with materialAfter the organic layer had been dried over anhydrous sodium sulfate
  8. customthe ether was evaporated
  9. distillationThe remaining liquid was purified by distillation at reduced pressure

출처 및 근거

ORD 기록
ord-c758642d4a244103b3b181cbb7b6cb05
출처 데이터셋
uspto-grants-1978_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04118505

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