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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetone → HCID 23367237, 화합물

HRID 1080186
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HRID 1080186 반응식
[CH3:1][C:2]1[S:3][CH2:4][CH2:5][N:6]=1.[Br:7][CH2:8][CH2:9][OH:10].CC(C)=O.CCOCC>O1CCOCC1>[Br-:7].[OH:10][CH2:9][CH2:8][N+:6]1[CH:5]=[CH:4][S:3][C:2]=1[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 180AcetoneHCID 3283Diethyl Ether2회HCID 108982-BromoethanolHCID 168672-Methyl-2-thiazoline

생성물 1

HCID 23367237HCID 23367237, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To a solution of 2-methylthiazoline (10.1 g) in dioxane (20 ml) was added 2-bromoethanol (13.8 g), and the mixture was heated under reflux for about 6 hours. After cooling the reaction, acetone (30 ml) and ether (130 ml) were added with stirring, and the resulting mixture was left standing. After the pale brown supernatant was discarded, ether (150 ml) was further added to the amorphous precipitate thus obtained. The mixture was stirred and left standing. Supernatant obtained was discarded, and the viscous precipitates obtained was left standing at an ambient temperature under reduced pressure to give the title compound as the yellow amorphous residue.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for about 6 hours
  3. temperatureAfter cooling
  4. additionwere added
  5. waitthe resulting mixture was left
  6. customthus obtained
  7. stirringThe mixture was stirred
  8. waitleft
  9. customSupernatant obtained
  10. customthe viscous precipitates
  11. customobtained
  12. waitwas left
  13. customstanding at an ambient temperature under reduced pressure

출처 및 근거

ORD 기록
ord-d8ac449be7624aadaab34d52356f45f4
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05580904

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