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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → HCID 54547883, 화합물

HRID 361489
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HRID 361489 반응식
[CH2:1]([OH:7])[CH2:2][CH2:3][CH:4]=[CH:5][CH3:6].[CH3:8][S:9](Cl)(=[O:11])=[O:10].C(N(CC)CC)C>ClCCl>[CH3:8][S:9]([O:7][CH2:1][CH2:2][CH2:3][CH:4]=[CH:5][CH3:6])(=[O:11])=[O:10]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 61370Hex-4-en-1-ol

생성물 1

HCID 54547883HCID 54547883, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

This example illustrates a synthesis of 1-(4,5-Oxohexyl)-3,7-dimethylxanthine (inventive compound no. 1555). To a solution of 4-hexen-1-ol (1.22 g, 12.2 mmol) and methanesulfonyl chloride (1.04 mL, 13.4 mmol) in dichloromethane (15 mL), cooled in an ice bath, was added triethylamine (2.55 mL, 18.3 mmol) dropwise. After 5 minutes, the cooling bath was removed and the mixture stirred for an additional 45 minutes and then treated with saturated aqueous sodium bicarbonate solution (25 mL). The layers were separated and the aqueous layer extracted with dichloromethane (20 mL). The combined organic layers were dried over magnesium sulfate and the solvents evaporated under vacuum, yielding 1-methanesulfonyloxy-4-hexene as a viscous oil.

후처리

  1. customthe cooling bath was removed
  2. additiontreated with saturated aqueous sodium bicarbonate solution (25 mL)
  3. customThe layers were separated
  4. extractionthe aqueous layer extracted with dichloromethane (20 mL)
  5. dry with materialThe combined organic layers were dried over magnesium sulfate
  6. customthe solvents evaporated under vacuum

출처 및 근거

ORD 기록
ord-4c4b634d10a24d28b88d9c8b46642a63
출처 데이터셋
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05866576

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