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Hydrochloric Acid → Methyl 1-Formylcyclopropane-1-carboxylate

HRID 1255436
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HRID 1255436 반응식
[C:1]1([C:8](OC)=[O:9])([C:4]([O:6][CH3:7])=[O:5])[CH2:3][CH2:2]1.CC(C[AlH]CC(C)C)C.[Cl-].[NH4+].Cl>ClCCl>[CH:8]([C:1]1([C:4]([O:6][CH3:7])=[O:5])[CH2:3][CH2:2]1)=[O:9]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 14487Diisobutylaluminum hydrideHCID 25517Ammonium ChlorideHCID 27695391,1-Cyclopropanedicarboxylic acid, 1,1-dimethyl ester

생성물 1

HCID 53415969Methyl 1-Formylcyclopropane-1-carboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
-78 °C

실험 절차

Dimethyl cyclopropane-1,1-dicarboxylate (6.90 ml, 50 mmol) was dissolved in dichloromethane (100 mL) and cooled to −78° C. DIBAL (1.0 M in DCM, 100 ml, 100 mmol) was added slowly over a period of 30 minutes. The reaction mixture was stirred for 6.5 hours at −78° C. then treated carefully with an aqueous saturated solution of ammonium chloride (16 mL) followed by HCl (1.0 M, 20 mL). The reaction was allowed to warm to room temperature over the weekend. The solids were filtered off and washed with DCM. The filtrate was washed with brine, dried over magnesium sulfate and the solvent removed under reduced pressure (200 mbar at rt). The crude product was purified on silica gel by flash column chromatography to afford the desired compound as a 45% w/w solution in EtOAc/DCM/ether as judged by 1H NMR (3.295 g).

후처리

  1. temperatureto warm to room temperature over the weekend
  2. filtrationThe solids were filtered off
  3. washwashed with DCM
  4. washThe filtrate was washed with brine
  5. dry with materialdried over magnesium sulfate
  6. customthe solvent removed under reduced pressure (200 mbar at rt)
  7. customThe crude product was purified on silica gel by flash column chromatography

출처 및 근거

ORD 기록
ord-7782b0e25a93409cb9116e48261575af
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08461149B2

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