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Hydrochloric Acid → Methyl 2-(prop-2-yn-1-yloxy)acetate

HRID 987375
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HRID 987375 반응식
[H-].[Na+].[CH2:3]([OH:6])[C:4]#[CH:5].Br[CH2:8][C:9]([O:11][CH3:12])=[O:10].Cl>O1CCCC1>[CH2:3]([O:6][CH2:8][C:9]([O:11][CH3:12])=[O:10])[C:4]#[CH:5]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 7859Propargyl alcoholHCID 24758Sodium hydrideHCID 60984Methyl bromoacetate

생성물 1

HCID 10877131Methyl 2-(prop-2-yn-1-yloxy)acetate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매3회

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온도
0 °C

실험 절차

A mechanically stirred suspension of sodium hydride (60 5% dispersion in mineral oil) (50 g, 1.25 mol) in tetrahydrofuran (800 mL) at 0° C. under nitrogen was treated dropwise with a solution of propargyl alcohol (84 g, 1.5 mol) in tetrahydrofuran (175 mL), stirred at 0° C. for 1 hour, treated with a solution of methyl bromoacetate in tetrahydrofuran (250 mL) over 15 minutes, stirred at 0° C. for 30 minutes, stirred at ambient temperature for 2 hours, and treated with 2M HCl (800 mL). The organic layer was isolated and the aqueous layer was extracted with ethyl acetate (2×, 500 mL). The combined organic layers were washed with brine (200 mL), dreid (MgSO4), filtered, concentrated and distilled (bp 75-85° C. at 20 torr) to provide the title compound (83 g).

후처리

  1. stirringstirred at 0° C. for 30 minutes
  2. stirringstirred at ambient temperature for 2 hours
  3. customThe organic layer was isolated
  4. extractionthe aqueous layer was extracted with ethyl acetate (2×, 500 mL)
  5. washThe combined organic layers were washed with brine (200 mL), dreid (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. distillationdistilled (bp 75-85° C. at 20 torr)

출처 및 근거

ORD 기록
ord-55f3c5b57dab45eebda83191eaac81da
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06632418B2

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