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Hydrochloric Acid → 4-(2-Methoxyethoxy)cyclohexanone

HRID 2060008
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HRID 2060008 반응식
Cl.[CH3:2][O:3][CH2:4][CH2:5][O:6][CH:7]1[CH2:16][CH2:15][C:10]2(OCC[O:11]2)[CH2:9][CH2:8]1>O1CCCC1>[CH3:2][O:3][CH2:4][CH2:5][O:6][CH:7]1[CH2:16][CH2:15][C:10](=[O:11])[CH2:9][CH2:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 594440998-(2-Methoxyethoxy)-1,4-dioxa-spiro[4.5]decane

생성물 1

HCID 138222284-(2-Methoxyethoxy)cyclohexanone수율 63%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

In a 10 L round-bottomed flask 8-{[2-(methyloxy)ethyl]oxy}-1,4-dioxaspiro[4.5]decane D60 (151 g, 700 mmol) was dissolved in tetrahydrofuran (THF) (3000 mL) to give a colourless solution. 3M hydrochloric acid (2333 mL, 7000 mmol) was added. Reaction was allowed to stir at room temperature overnight. The organic solvent was partially evaporated under vacuum and then the aqueous layer was back extracted with DCM (3×500 mL). The organic phase was dried over Na2SO4, filtered and concentrated to obtain 121 g of crude material as yellow oil. The crude product was purified by Biotage® 75 L SiO2 column eluting with c-hex/EtOAc 8/2 to get title material (76 g; 63%).

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후처리

  1. customto give a colourless solution
  2. customReaction
  3. customThe organic solvent was partially evaporated under vacuum
  4. extractionthe aqueous layer was back extracted with DCM (3×500 mL)
  5. dry with materialThe organic phase was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto obtain 121 g of crude material as yellow oil
  9. customThe crude product was purified by Biotage® 75 L SiO2 column
  10. washeluting with c-hex/EtOAc 8/2

출처 및 근거

ORD 기록
ord-444ab46f721042a3a4796b0a4ef3e67f
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08278328B2

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