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

Iodine → 6-(3-Methylidenepentyl)-1,4-dioxepan-6-ol

HRID 647744
노트
인쇄 미리보기

반응식

HRID 647744 반응식
[Mg].II.Br[CH2:5][CH2:6]Br.Cl[CH2:9][C:10](CCl)(CCl)[CH2:11][CH3:12].[O:17]1[CH2:23][C:22](=[O:24])[CH2:21][O:20][CH:19]=[CH:18]1.[Cl-].[NH4+]>O1CCCC1.C(OCC)C>[CH2:9]=[C:10]([CH2:5][CH3:6])[CH2:11][CH2:12][C:22]1([OH:24])[CH2:21][O:20][CH2:19][CH2:18][O:17][CH2:23]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 6

HCID 807IodineHCID 78391,2-DibromoethaneHCID 25517Ammonium ChlorideHCID 35664471,1,1-Tris(chloromethyl)propane2회HCID 5462224MagnesiumHCID 132371731,4-Dioxepin-6-one

생성물 1

HCID 132371746-(3-Methylidenepentyl)-1,4-dioxepan-6-ol

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매4회

반응 조건

온도
-60 °C

실험 절차

To 0.99 g of dry magnesium shavings was added 14 ml of dry tetrahydrofuran and a small crystal of iodine. After 20 minutes, 0.25 ml of 1,2-dibromoethane was added by syringe and then 0.5 ml of a 70% tetrahydrofuran solution of 1,1,1-tris(chloromethyl)propane. The reaction mixture was warmed to reflux and more 70% 1,1,1-tris(chloromethyl)propane solution was added to total 5.29 g at a rate to maintain reflux. After the addition was complete, the reaction was refluxed for an additional half hour. After the addition of 10 ml of tetrahydrofuran, the reaction mixture was cooled to -60° C. and 2.06 g of 1,4-dioxepin-6-one in 10 ml of tetrahydrofuran was added dropwise. After 2.5 hours at -60° C., the reaction mixture was warmed to -20° C. and poured into a mixture of 200 ml of saturated ammonium chloride and diethyl ether. The resulting layers were separated and the aqueous layer was extracted twice with diethyl ether. The combined organic layers were washed with water, dried and stripped to yield 3.05 g of the desired product as a dark yellow liquid.

후처리

  1. temperatureThe reaction mixture was warmed
  2. temperatureto reflux
  3. temperatureto maintain
  4. temperaturereflux
  5. additionAfter the addition
  6. temperaturethe reaction was refluxed for an additional half hour
  7. waitAfter 2.5 hours at -60° C.
  8. temperaturethe reaction mixture was warmed to -20° C.
  9. customThe resulting layers were separated
  10. extractionthe aqueous layer was extracted twice with diethyl ether
  11. washThe combined organic layers were washed with water
  12. customdried

출처 및 근거

ORD 기록
ord-eb66837cab6942efa9d05f30107eeb08
출처 데이터셋
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04410354

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트