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Hydrochloric Acid → 5-[(Methoxycarbonyl)amino]pentanoic acid

HRID 459026
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HRID 459026 반응식
Cl.[NH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([OH:9])=[O:8].C(=O)([O-])[O-].[K+].[K+].Cl[C:17]([O:19][CH3:20])=[O:18].Cl>O.O1CCOCC1>[CH3:20][O:19][C:17]([NH:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([OH:9])=[O:8])=[O:18]
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 6586Methyl chloroformateHCID 11430Potassium CarbonateHCID 693985-Aminovaleric acid hydrochloride

생성물 1

HCID 184429725-[(Methoxycarbonyl)amino]pentanoic acid수율 65.9%

시약·촉매·용매 2

HCID 962Water용매2회
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 31275
1,4-Dioxane
용매

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온도
0 °C

실험 절차

5-Aminopentanoic acid hydrochloride (2 g, 13 mmol), and potassium carbonate (13 g, 94 mmol) were dissolved in water (30 ml) and dioxane (10 ml) then cooled to 0° C. Methyl chloroformate (5 ml, 65 mmol) was added over 30 seconds, then the mixture was stirred for 2.5 hours at 0° C. Concentrated HCl was added until the mixture became acidic then the mixture was diluted with water and extracted with ether. The organic layer was dried over magnesium sulfate, evaporated and dried in vacuo to give 5-[(methoxycarbonyl)amino]pentanoic acid as a white powder (1.5 g).

후처리

  1. extractionextracted with ether
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. customevaporated
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-9f9e4cbb0d144909877185776fdc134d
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07192974B2

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