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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Triethylamine → HCID 54547883、化合物

HRID 1954104
ノート
印刷プレビュー

反応式

HRID 1954104 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 54547883HCID 54547883、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-4d2cd7dcc76544a1bd884d1172554482
出典データセット
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06121270

反応ノート

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