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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sulfuric Acid → N-methylaspartic acid sulfate

HRID 39211
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HRID 39211 반응식
[CH3:1][NH:2][C@H:3]([C:8]([OH:10])=[O:9])[CH2:4][C:5]([OH:7])=[O:6].[S:11](=[O:15])(=[O:14])([OH:13])[OH:12]>O>[S:11]([OH:15])([OH:14])(=[O:13])=[O:12].[CH3:1][NH:2][C@H:3]([C:8]([OH:10])=[O:9])[CH2:4][C:5]([OH:7])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1118Sulfuric AcidHCID 92982N-Methyl-L-aspartic acid

생성물 1

HCID 86639894N-methylaspartic acid sulfate수율 95.5%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

10.7 g of N-methylaspartic acid was placed in a 250 ml round-bottom flask, and 100 ml of water was added to the flask and stirred for 30 minutes by using a magnetic stirrer. 7.12 g of concentrate sulfuric acid (concentration: 98%) was slowly dropped into the flask under stirring, and stirred for additional 2 hours after dropping. After the reaction, the reaction solution was concentrated, azeotroped with 100 ml of toluene to further remove the water and dried under vacuum to obtain 17 g of N-methylaspartic acid sulfate as yellow oil (Yield: 95.3%).

후처리

  1. stirringunder stirring
  2. stirringstirred for additional 2 hours
  3. customAfter the reaction
  4. concentrationthe reaction solution was concentrated
  5. customazeotroped with 100 ml of toluene
  6. customto further remove the water
  7. customdried under vacuum

출처 및 근거

ORD 기록
ord-53db3abe415442db8d58a89781f64b4c
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524895B2

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