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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 10219783, 화합물

HRID 650114
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HRID 650114 반응식
[C:1]([NH:5][C:6](=[O:17])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[O:13]C(=O)C)([CH3:4])([CH3:3])[CH3:2].O.Cl>C1COCC1>[C:1]([NH:5][C:6](=[O:17])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[OH:13])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric Acid2회HCID 962WaterHCID 1279601HCID 1279601, 화합물

생성물 1

HCID 10219783HCID 10219783, 화합물수율 80.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The product from Step A (2.35 g, 0.010 mol) was dissolved in THF wand 10 mL of water was added to form a clear suspension. Hydrochloric acid (5%) was added until the solution reached a pH˜1. The reaction mixture was then refluxed for 24 hours. TLC indicated that about half of the starting material remained, so an additonal 10 mL of 5% hydrochloric acid was added and the reaction mixture was refluxed for 24 hours. The THF was then removed by rotoevaporation and the remaining aqueous mixture was extracted with hexanes (2×20 mL). The combined hexane layers were washed with water (2×40 mL), dried over MgSO4 and the hexane removed in vacuo to provide 1.56 g (80.8% yield) of the title compound as a white crystalline solid, m.p. 78-79.5° C.

후처리

  1. additionwas added
  2. customto form a clear suspension
  3. temperatureThe reaction mixture was then refluxed for 24 hours
  4. additionwas added
  5. temperaturethe reaction mixture was refluxed for 24 hours
  6. customThe THF was then removed by rotoevaporation
  7. extractionthe remaining aqueous mixture was extracted with hexanes (2×20 mL)
  8. washThe combined hexane layers were washed with water (2×40 mL)
  9. dry with materialdried over MgSO4
  10. customthe hexane removed in vacuo

출처 및 근거

ORD 기록
ord-0693be00f88a48e58e7d7636c98dab9e
출처 데이터셋
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06271265B1

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