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HCID 2749395, 화합물 → Diethyl 3,3'-(1,3-phenylene)dipropanoate

HRID 225791
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인쇄 미리보기

반응식

HRID 225791 반응식
[CH2:1]([O:3][C:4](=[O:20])[CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([CH:13]=[CH:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH:8]=1)[CH3:2]>CO.[Pd]>[CH2:1]([O:3][C:4](=[O:20])[CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([CH2:13][CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH:8]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 2749395HCID 2749395, 화합물

생성물 1

HCID 69039070Diethyl 3,3'-(1,3-phenylene)dipropanoate수율 94%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A stirred solution of the intermediate from Step A (6.5 g, 23.7 mmol) in MeOH (300 mL) was flushed with nitrogen gas and palladium (650 mg; 10 wt. % (dry basis) on activated carbon) was added. The reaction flask was then placed under vacuum and flushed with hydrogen gas (3 cycles). The reaction mixture was stirred overnight (16 hours) and then flushed with nitrogen gas. The mixture was filtered and the solvent removed under reduced pressure to provide 6.2 g of the title intermediate (94% yield), which was used without further purification.

후처리

  1. additionwas added
  2. customflushed with hydrogen gas (3 cycles)
  3. customflushed with nitrogen gas
  4. filtrationThe mixture was filtered
  5. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-c4f4d4c7c3e343e8844854e4c6f276b5
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07557126B2

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