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Iodoethane → Ethyl 5-(ethoxymethyl)-4,5-dihydroisoxazole-3-carboxylate

HRID 58540
ノート
印刷プレビュー

反応式

HRID 58540 の反応式
[H-].[Na+].[OH:3][CH2:4][CH:5]1[O:9][N:8]=[C:7]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH2:6]1.I[CH2:16][CH3:17]>CN(C=O)C>[CH2:16]([O:3][CH2:4][CH:5]1[O:9][N:8]=[C:7]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH2:6]1)[CH3:17]
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 6340IodoethaneHCID 24758Sodium hydrideHCID 23643400Ethyl 5-(hydroxymethyl)-4,5-dihydro-1,2-oxazole-3-carboxylate

生成物 1

HCID 66831765Ethyl 5-(ethoxymethyl)-4,5-dihydroisoxazole-3-carboxylate収率 40.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Sodium hydride (0.141 g; 3.51 mmol) was added to a solution of ethyl 5-(hydroxymethyl)-4,5-dihydroisoxazole-3-carboxylate (0.338 g; 1.76 mmol) in DMF (3 mL) in an ice bath. The mixture was stirred for 10 min before addition of iodoethane (0.430 mL; 5.27 mmol). The ice bath was removed and the mixture was stirred at room temperature for 2 h. After evaporation, the residue was partitioned between brine and dichloromethane and the solution extracted with dichloromethane. Organic extracts were evaporated and the residue was purified by flash chromatography on silica gel (eluent: 1-6% ethyl acetate in dichloromethane) to afford 0.142 g (40%) of ethyl 5-(ethoxymethyl)-4,5-dihydroisoxazole-3-carboxylate.

後処理

  1. customThe ice bath was removed
  2. customAfter evaporation
  3. customthe residue was partitioned between brine and dichloromethane
  4. extractionthe solution extracted with dichloromethane
  5. customOrganic extracts were evaporated
  6. customthe residue was purified by flash chromatography on silica gel (eluent: 1-6% ethyl acetate in dichloromethane)

出典と根拠

ORDレコード
ord-c02caa71ff834a129605d4fc49a44f1b
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09434722B2

反応ノート

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