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Methyl chloroglyoxylate → HCID 57904866, 화합물

HRID 1093034
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HRID 1093034 반응식
Cl.[F:2][CH2:3][CH2:4][NH:5][CH3:6].C(N(C(C)C)CC)(C)C.Cl[C:17](=[O:22])[C:18]([O:20][CH3:21])=[O:19]>C(Cl)Cl>[F:2][CH2:3][CH2:4][N:5]([CH3:6])[C:17](=[O:22])[C:18]([O:20][CH3:21])=[O:19]
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참가 물질

5

반응물 3

HCID 79846Methyl chloroglyoxylateHCID 81531DiisopropylethylamineHCID 85799809(2-Fluoroethyl)(methyl)amine hydrochloride

생성물 1

HCID 57904866HCID 57904866, 화합물수율 92%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 2-fluoro-N-methylethanamine hydrochloride salt (1 g, 8.81 mmol) in CH2Cl2 (40.0 mL) was added drop-wise diisopropyl-ethylamine (5.59 mL, 32.0 mmol) followed by the drop-wise addition of methyl 2-chloro-2-oxoacetate (0.981 g, 8.01 mmol) and the resulting mixture stirred for 3 h under N2. The solution was concentrated and the residue was taken up in ethyl acetate (20 mL), washed with 1N HCl (2×15 mL) followed by saturated aqueous sodium bicarbonate (15 mL). The organic phase was dried (MgSO4), filtered, and concentrated to give the title compound as a clear oil (1.2 g, 92% yield). 1H NMR (500 MHz, CDCl3) δ: 4.46-4.73 (2 H, m) 3.82-3.93 (3 H, m) 3.60-3.77 (2 H, m) 3.01-3.20 (3 H, m). LCMS (M+H) calcd for C6H11FNO3: 164.07; found: 164.11.

후처리

  1. concentrationThe solution was concentrated
  2. washwashed with 1N HCl (2×15 mL)
  3. dry with materialThe organic phase was dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-be13b1f862704e7ca95fc9d58f559846
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08129398B2

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