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Diethyl Malonate → HCID 67099102, 화합물

HRID 1868628
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HRID 1868628 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:13])([CH3:12])[C:9]([OH:11])=O)=[CH:4][CH:3]=1.C(Cl)(=O)C(Cl)=O.[C:20]([O:28][CH2:29][CH3:30])(=[O:27])[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23].[Mg+2].[Cl-].[Cl-].C([O-])(=O)CC([O-])=O>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([CH3:13])([CH3:12])[C:9]([CH:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[C:20]([O:28][CH2:29][CH3:30])=[O:27])=[O:11])=[CH:6][CH:7]=1
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참가 물질

7

반응물 5

HCID 7761Diethyl MalonateHCID 9084Malonate IonHCID 65578Oxalyl chlorideHCID 804062-(4-Chlorophenyl)-2-methylpropionic acidHCID 5360315Magnesium Chloride

생성물 1

HCID 67099102HCID 67099102, 화합물

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

A solution of 2-(4-chlorophenyl)-2-methylpropionic acid (1.99 g, 10.0 mmol, 1.0 eq.) in IPAc (10 mL) was treated with DMF (0.02 mL) and oxalyl chloride (0.92 mL, 10.5 mmol). The resulting solution was stirred at room temperature for 2 hours. In a separate vessel, was charged diethyl malonate (1.91 mL, 12.5 mmol), IPAc (14 mL), and MgCl2 (11.9 g, 12.5 mmol). The resulting malonate slurry was stirred at room temperature for 30 minutes and subsequently treated with TEA (4.7 mL, 33.5 mmol). The resulting suspension was aged at room temperature for 2 hours, cooled to 5° C. and treated with the above acyl chloride solution. The resulting mixture was warmed to ambient temperature and aged for 1 hour. The slurry was quenched with a 5N HCl solution (10 mL) and the phases were split. The organic phase was washed with saturated NaHCO3 solution (2×10 mL) and water (1×10 mL). The organic phase was dried (MgSO4) and concentrated in vacuo to afford an orange oil. MS m/e=341.2 (M+H)+.

후처리

  1. waitThe resulting suspension was aged at room temperature for 2 hours
  2. temperaturecooled to 5° C.
  3. temperatureThe resulting mixture was warmed to ambient temperature and aged for 1 hour
  4. customThe slurry was quenched with a 5N HCl solution (10 mL)
  5. customthe phases were split
  6. washThe organic phase was washed with saturated NaHCO3 solution (2×10 mL) and water (1×10 mL)
  7. dry with materialThe organic phase was dried (MgSO4)
  8. concentrationconcentrated in vacuo
  9. customto afford an orange oil

출처 및 근거

ORD 기록
ord-49de6bd3743342abbef273385eb46931
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07635715B2

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