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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Chloroacetic Acid → HCID 43700001, 화합물

HRID 2075510
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HRID 2075510 반응식
[Cl:1][CH2:2][C:3](O)=[O:4].[CH3:6][O:7][C:8](=[O:13])[C:9]([NH2:12])([CH3:11])[CH3:10].C(N(CC)C(C)C)(C)C>C1COCC1>[CH3:6][O:7][C:8](=[O:13])[C:9]([NH:12][C:3](=[O:4])[CH2:2][Cl:1])([CH3:11])[CH3:10]
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참가 물질

5

반응물 3

HCID 300Chloroacetic AcidHCID 81531DiisopropylethylamineHCID 4186341Methyl 2-amino-2-methylpropanoate

생성물 1

HCID 43700001HCID 43700001, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 0.95 g chloro acetic acid in 20 ml of dry THF 1.78 g N,N′-carbonyl-diimidazole were added. After 0.5 h at room temperature and under argon atmosphere 1.69 g 2-amino-2-methyl-propionic acid methyl ester and 1.29 g N,N-diisopropyl-ethyl-amine were added and it was stirred for 3 h. Then the solvent was evaporated, the residue taken up in ethyl acetate and washed with 2 M hydrochloric acid, water and sat. aqueous sodium hydrogen carbonate solution. The combined organic fractions were dried over sodium sulphate, filtrated and concentrated. The resulting residue was crystallized from diethylether to yield 2-(2-chloro-acetylamino)-2-methyl-propionic acid methyl ester.

후처리

  1. customThen the solvent was evaporated
  2. washwashed with 2 M hydrochloric acid, water and sat. aqueous sodium hydrogen carbonate solution
  3. dry with materialThe combined organic fractions were dried over sodium sulphate
  4. filtrationfiltrated
  5. concentrationconcentrated
  6. customThe resulting residue was crystallized from diethylether

출처 및 근거

ORD 기록
ord-46d07f2a603a4418be0d1af82d6fa4d2
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07919628B2

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