홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Hydrogen Bromide → HCID 14646171, 화합물

HRID 371167
노트
인쇄 미리보기

반응식

HRID 371167 반응식
[OH:1][CH2:2][C:3]([CH2:8][OH:9])([CH2:6][OH:7])[CH2:4][OH:5].[BrH:10].C(OC(=O)C)(=O)C>C(O)(=O)C>[Br:10][CH:2]([C:3]([CH2:8][OH:9])([CH2:6][OH:7])[CH2:4][OH:5])[OH:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 260Hydrogen Bromide3회HCID 7918Acetic Anhydride2회HCID 8285Pentaerythritol2회

생성물 1

HCID 14646171HCID 14646171, 화합물수율 70%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

In a 2 liter, three-necked flask equipped with a reflux condenser and an addition funnel are placed 200 g pentaerythritol (1.47 mole) and 16 ml 48% hydrobromic acid in about 500 ml glacial acetic acid. The mixture is refluxed for about one-half hour until all pentaerythritol is dissolved. Then, 170 ml 48% hydrobromic acid are added, followed by 310 ml acetic anhydride and the mixture is refluxed for 3 hours. Then, 94 ml 48% hydrobromic acid followed by 150 ml acetic anhydride are added and the mixture is refluxed for an additional 3 hours. The acetic acid is then removed as completely as possible on a rotary evaporator. Ethanol (95%, 750 ml) and 17 ml 48% hydrobromic acid are then added to the residue. The flask is equipped with 1 m Vigreux column and the azeotrope ethyl acetate/ethanol is slowly distilled off. When 500 ml distillate has been collected, an additional 750 ml 95% ethanol is added and the distillation is continued until about 400 ml is left over. After cooling, the precipitated pentaerythritol is filtered off. The solvent is evaporated and the residue is dissolved in water. The aqueous phase is extracted twice with carbon tetrachloride and twice with ether. The water is evaporated on the rotary evaporator and the last traces of water are removed by azeotropic distillation with toluene using a Dean-Stark trap. The solid is recrystallized from chloroform containing 10% acetonitrile. The first crop yielded 190 g monobromopentaerythritol. The total yield is 70%.

후처리

  1. customIn a 2 liter, three-necked flask equipped with a reflux condenser and an addition funnel
  2. dissolutionis dissolved
  3. temperaturethe mixture is refluxed for 3 hours
  4. additionare added
  5. temperaturethe mixture is refluxed for an additional 3 hours
  6. customThe acetic acid is then removed as completely as
  7. custompossible on a rotary evaporator
  8. additionEthanol (95%, 750 ml) and 17 ml 48% hydrobromic acid are then added to the residue
  9. customThe flask is equipped with 1 m Vigreux column
  10. distillationthe azeotrope ethyl acetate/ethanol is slowly distilled off
  11. distillationWhen 500 ml distillate has been collected
  12. additionan additional 750 ml 95% ethanol is added
  13. distillationthe distillation
  14. waitis left over
  15. temperatureAfter cooling
  16. filtrationthe precipitated pentaerythritol is filtered off
  17. customThe solvent is evaporated
  18. dissolutionthe residue is dissolved in water
  19. extractionThe aqueous phase is extracted twice with carbon tetrachloride and twice with ether
  20. customThe water is evaporated on the rotary evaporator
  21. customthe last traces of water are removed by azeotropic distillation with toluene using a Dean-Stark trap
  22. customThe solid is recrystallized from chloroform containing 10% acetonitrile

출처 및 근거

ORD 기록
ord-7a2721dcf98d4711ab20c3c547bb59de
출처 데이터셋
uspto-grants-1985_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04529786

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트