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Methanol → N-(2-hydroxyethyl)-2-iodo-4,5-dimethoxybenzamide

HRID 2175713
ノート
印刷プレビュー

反応式

HRID 2175713 の反応式
[Li+].[BH4-].[I:3][C:4]1[CH:18]=[C:17]([O:19][CH3:20])[C:16]([O:21][CH3:22])=[CH:15][C:5]=1[C:6]([NH:8][CH2:9][C:10](OCC)=[O:11])=[O:7].CO>C1COCC1>[OH:11][CH2:10][CH2:9][NH:8][C:6](=[O:7])[C:5]1[CH:15]=[C:16]([O:21][CH3:22])[C:17]([O:19][CH3:20])=[CH:18][C:4]=1[I:3]
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 887MethanolHCID 4148881Lithium borohydrideHCID 67087805Ethyl 2-(2-iodo-4,5-dimethoxybenzamido)acetate

生成物 1

HCID 67087759N-(2-hydroxyethyl)-2-iodo-4,5-dimethoxybenzamide収率 80%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

LiBH4 (63 mg, 3 mmol) was added to a stirred solution of ethyl 2-(2-iodo-4,5-dimethoxybenzamido)acetate (379 mg, 1 mmol) in THF (2 mL) at −10° C. The reaction was stirred for 5 min then methanol (0.22 mL) was added dropwise. The reaction mixture was warmed to room temperature, stirred for 30 minutes and quenched by addition of water. The THF was removed under reduced pressure and the aqueous residue was thoroughly extracted with DCM. The combined organic phases were washed with brine, dried over sodium sulphate and evaporated to give the crude product which was purified by re-crystallization from EtOAc and hexane to give N-(2-hydroxyethyl)-2-iodo-4,5-dimethoxybenzamide (280 mg, 80%) LC-MS (ES-API); rt 7.60 min; m/z calculated for C11H14NO4 [M+H]+ 352.0, found 352.0.

後処理

  1. stirringstirred for 30 minutes
  2. customquenched by addition of water
  3. customThe THF was removed under reduced pressure
  4. extractionthe aqueous residue was thoroughly extracted with DCM
  5. washThe combined organic phases were washed with brine
  6. dry with materialdried over sodium sulphate
  7. customevaporated
  8. customto give the crude product which
  9. customwas purified by re-crystallization from EtOAc and hexane

出典と根拠

ORDレコード
ord-8bbe94b36b2649158f1399693258bab5
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09062076B2

反応ノート

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