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Sodium Hydroxide → 4-Chloro-3-isobutyl-but-3-en-2-one

HRID 1676106
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HRID 1676106 반응식
O[CH:2]=[C:3]([CH2:7][CH:8]([CH3:10])[CH3:9])[C:4](=[O:6])[CH3:5].C(Cl)(=O)C([Cl:14])=O.[OH-].[Na+]>C(Cl)(Cl)Cl>[Cl:14][CH:2]=[C:3]([CH2:7][CH:8]([CH3:10])[CH3:9])[C:4](=[O:6])[CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 65578Oxalyl chlorideHCID 866457654-Hydroxy-3-isobutyl-but-3-en-2-one

생성물 1

HCID 866457664-Chloro-3-isobutyl-but-3-en-2-one수율 99.9%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

To a solution of 4-hydroxy-3-isobutyl-but-3-en-2-one (28 g, 197 mmol) in chloroform (350 mL) a soution of oxalylchloride (44.3 g, 349 mmol) in chloroform (50 mL) is added slowly during 5 min. The resulting dark brown mixture is stirred at rt for 2 h before it is cooled to 0° C. and treated with ice (100 g) followed by 1 N aq. NaOH (100 mL). When the quite violent gas evolution ceases the phases are separated (the still acidic aq. phase is discarded). The organic phase is washed with 1N aq. NaOH (3×75 mL) and 1 N aq. NaH2PO4 (75 mL), dried (MgSO4), filtered and evaporated to give crude 4-chloro-3-isobutyl-but-3-en-2-one (31.6 g) as a dark brown oil; LC-MS: tR=0.97 min.

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후처리

  1. temperatureis cooled to 0° C.
  2. customare separated (the still acidic aq. phase
  3. washThe organic phase is washed with 1N aq. NaOH (3×75 mL) and 1 N aq. NaH2PO4 (75 mL)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customevaporated

출처 및 근거

ORD 기록
ord-04b7007b60aa4fd7966a7dbb7468942c
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08003800B2

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