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Triethylamine → 4-(2-Fluorobenzoyl)-3-(hydroxymethyl)morpholine

HRID 969264
ノート
印刷プレビュー

反応式

HRID 969264 の反応式
[OH:1][CH2:2][CH:3]1[CH2:8][O:7][CH2:6][CH2:5][NH:4]1.[F:9][C:10]1[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=1[C:12](Cl)=[O:13].C(N(CC)CC)C.[OH-].[Na+]>ClCCl>[F:9][C:10]1[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=1[C:12]([N:4]1[CH2:5][CH2:6][O:7][CH2:8][CH:3]1[CH2:2][OH:1])=[O:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8471TriethylamineHCID 98082-Fluorobenzoyl chlorideHCID 14798Sodium HydroxideHCID 5058360(Morpholin-3-yl)methanol

生成物 1

HCID 690585764-(2-Fluorobenzoyl)-3-(hydroxymethyl)morpholine収率 2,339%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 3-(hydroxymethyl)morpholine (345 mg; 2.95 mmol) in dichloromethane (10 mL) was carefully added 2-fluorobenzoyl chloride (0.35 mL; 2.95 mmol) and triethylamine (0.62 mL; 4.42 mmol) and the reaction stirred for 0.5 h. The product was combined with 4 N NaOH (10 mL) to hydrolyse any ester and the organic layer extracted (dichloromethane, 3×). The combined organic layers were dried (Na2SO4) and the solvent evaporated to give an oil, which was purified by flash column chromatography on silica (gradient elution, dichloromethane-methanol 1:0 to 9:1) to give 4-(2-fluorobenzoyl)-3-(hydroxymethyl)morpholine (165 mg; o.69 mmol), EIMS: m/z=240.2 (M+H)+. This product and caesium carbonate (0.544 g) were heated to 120° C. in dimethylformamide (10 ml) solution under nitrogen for 4 hours. The solvent was evaporated, and the residue taken up in water and extracted with dichloromethane (3×). The combined dichloromethane extracts were dried (Na2SO4) and the solvent evaporated to give a crude solid which was purified by flash column chromatography on silica, eluting with ether to give the title compound (77 mg). M.p. 105-107° C.; EIMS: m/z=220.2 (M+H)+.

後処理

  1. extractionthe organic layer extracted (dichloromethane, 3×)
  2. dry with materialThe combined organic layers were dried (Na2SO4)
  3. customthe solvent evaporated
  4. customto give an oil, which
  5. customwas purified by flash column chromatography on silica (gradient elution, dichloromethane-methanol 1:0 to 9:1)

出典と根拠

ORDレコード
ord-7b5e9560c3b44d49b1bfeb4e16143e12
出典データセット
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07307073B2

反応ノート

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