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

HRID 2175713
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HRID 2175713 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 4148881Lithium borohydrideHCID 67087805Ethyl 2-(2-iodo-4,5-dimethoxybenzamido)acetate

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-8bbe94b36b2649158f1399693258bab5
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062076B2

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