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Hydrochloric Acid → HCID 66840740, 화합물

HRID 468146
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HRID 468146 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[OH-].[K+].[CH3:12][CH2:13][C:14](=[O:17])[CH2:15][CH3:16].Cl>O>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[C:13]([CH3:12])[C:14](=[O:17])[CH2:15][CH3:16])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 7288Ethyl ketoneHCID 77264-ChlorobenzaldehydeHCID 14797Potassium Hydroxide

생성물 1

HCID 66840740HCID 66840740, 화합물수율 41.3%

시약·촉매·용매 1

HCID 962Water용매

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
65 °C

실험 절차

To 4-chlorobenzaldehyde 46a (99.6 mmol, 14 g) in water (44 mL) was added KOH (44.6 mmol, 2.5 g). The mixture was heated at 65° C. and 3-pentanone (99.6 mmol, 8.58 g) was added dropwise over 10 min. After refluxing for 8 h, the reaction mixture was cooled to room temperature and stirred overnight. Following addition of 260 mL 1N aqueous HCl, the mixture was extracted with EtOAc. The organic layer was dried over Na2SO4 and concentrated. The crude product was purified by flash column chromatography (silica gel, 5% EtOAc/heptane) to give 8.59 g of 46b.

후처리

  1. temperatureAfter refluxing for 8 h
  2. temperaturethe reaction mixture was cooled to room temperature
  3. extractionthe mixture was extracted with EtOAc
  4. dry with materialThe organic layer was dried over Na2SO4
  5. concentrationconcentrated
  6. customThe crude product was purified by flash column chromatography (silica gel, 5% EtOAc/heptane)

출처 및 근거

ORD 기록
ord-f1073f31c3cd485b88dd8617a77ea284
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08623858B2

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