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3-Hydroxybenzyl alcohol → 2-[3-(Hydroxymethyl)phenoxy]acetamide

HRID 594992
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HRID 594992 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][OH:6].Br[CH2:11][C:12]([NH2:14])=[O:13].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[OH:6][CH2:5][C:4]1[CH:3]=[C:2]([CH:9]=[CH:8][CH:7]=1)[O:1][CH2:11][C:12]([NH2:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1023-Hydroxybenzyl alcoholHCID 11430Potassium CarbonateHCID 696322-Bromoacetamide

생성물 1

HCID 9273882-[3-(Hydroxymethyl)phenoxy]acetamide수율 43%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of 3-hydroxybenzyl alcohol (500 mg, 4 mmol) in acetonitrile (10 mL) was added 2-bromoacetamide (1 eq) and potassium carbonate (1 eq). The resulting suspension was stirred at rt for 18 h. The solvent was removed in vacuo and the residue partitioned between EtOAc and H2O. The aqueous layer was acidified with dilute HCl (2M) and then re-extracted with EtOAc (3×50 mL). The organic phases were combined, dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography (EtOAc: methanol) to give 2-(3-(hydroxymethyl)phenoxy)acetamide (320 mg, 43%).

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후처리

  1. customThe solvent was removed in vacuo
  2. customthe residue partitioned between EtOAc and H2O
  3. extractionre-extracted with EtOAc (3×50 mL)
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe resultant residue was purified by column chromatography (EtOAc: methanol)

출처 및 근거

ORD 기록
ord-eecaca7346c444e6b2c0cd595518b658
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242987B2

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