Hydrochloric Acid → N-methoxy-N-methyl-2-(thiophen-3-yl)acetamide

HRID 401134노트

반응식

HRID 401134 반응식
[S:1]1[CH:5]=[CH:4][C:3]([CH2:6][C:7]([OH:9])=O)=[CH:2]1.[CH3:10][O:11][NH:12][CH3:13].CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1.Cl>C(Cl)Cl.C([O-])(O)=O.[Na+].[Cl-].[Na+].O>[CH3:10][O:11][N:12]([CH3:13])[C:7](=[O:9])[CH2:6][C:3]1[CH:4]=[CH:5][S:1][CH:2]=1

참가 물질

9

반응물 5

HCID 313Hydrochloric AcidHCID 14232N,O-DimethylhydroxylamineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 234043-Thiophenacetic acidHCID 757711-Hydroxybenzotriazole

생성물 1

HCID 11423995N-methoxy-N-methyl-2-(thiophen-3-yl)acetamide수율 76.6%

시약·촉매·용매 3

HCID 6344Dichloromethane용매2회HCID 516892Sodium Bicarbonate용매HCID 57417360Sodium chloride; water용매

실험 절차

A mixture of 2-(thiophen-3-yl)acetic acid (2.0 g, 14.1 mmol), O,N-dimethyl-hydroxylamine (1.68 g, 16.9 mmol), EDCI (2.95 g, 15.5 mmol), HOBT (2.15 g, 15.5 mmol), and TEA (3.7 mL, 31 mmol) in anhydrous DCM (50 mL) was stirred at room temperature under nitrogen for two hours. The reaction mixture was diluted with CH2Cl2, and the organic layer was washed with aqueous HCl solution (0.5 mol/L1, 30 mL×2), saturated NaHCO3 (30 mL×2) and brine (30 mL), dried over Na2SO4, filtered, and concentrated to give the crude N-methoxy-N-methyl-2-(thiophen-3-yl)acetamide (2.0 g, yield 76.6%).

후처리

  1. dry with materialdried over Na2SO4
  2. filtrationfiltered
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-bc976ee6f9594c499e53b84a9e59c8ee
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08741915B2

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