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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 2-(Morpholin-4-yl)acetic acid hydrochloride

HRID 61299
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HRID 61299 반응식
[O:1]1[CH2:6][CH2:5][N:4]([CH2:7][C:8]([O:10]C(C)(C)C)=[O:9])[CH2:3][CH2:2]1.[ClH:15]>O1CCOCC1.C(OCC)C>[ClH:15].[O:1]1[CH2:6][CH2:5][N:4]([CH2:7][C:8]([OH:10])=[O:9])[CH2:3][CH2:2]1
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 104428104-Morpholineacetic acid, 1,1-dimethylethyl ester

생성물 1

HCID 177509462-(Morpholin-4-yl)acetic acid hydrochloride

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 312751,4-Dioxane용매

실험 절차

Tert-butyl 2-morpholinoacetate (11 g, 54.7 mmol) was stirred with HCl, 4M in dioxane (54 mL), giving a white precipitate (a mild exotherm was observed) which slowly dissolved with stirring at room temperature. Ten minutes after complete dissolution, the mixture solidified. Then the mixture was warmed to 60° C. and the thick suspension was stirred vigorously overnight. The mixture was then cooled to room temperature, diluted with diethyl ether (60 mL) and filtered to collect the title compound (8 g, 80%) as a white solid. 1H NMR (CD3OD, 400 MHz): δ (ppm) 4.13 (s, 2H), 3.94 (brm, 4H), 3.41 (brm, 4H).

후처리

  1. customgiving a white precipitate (a mild exotherm
  2. dissolutionslowly dissolved
  3. dissolutionTen minutes after complete dissolution
  4. temperatureThen the mixture was warmed to 60° C.
  5. stirringthe thick suspension was stirred vigorously overnight
  6. temperatureThe mixture was then cooled to room temperature
  7. filtrationfiltered
  8. customto collect the title compound (8 g, 80%) as a white solid

출처 및 근거

ORD 기록
ord-39f24acd253746de84cead7c8fabe78f
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09441012B2

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