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

Ethanol → 3-O-Ethylascorbic acid

HRID 1175199
노트
인쇄 미리보기

반응식

HRID 1175199 반응식
[CH2:1]([O:3][C:4]1[C@@H:9]([C@H:10]([C:12](=C(C)C)[OH:13])[OH:11])[O:8][C:6](=[O:7])[C:5]=1[OH:17])[CH3:2].C(O)C>O.Cl>[CH2:1]([O:3][C:4]1[C@@H:9]([C@H:10]([CH2:12][OH:13])[OH:11])[O:8][C:6](=[O:7])[C:5]=1[OH:17])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 702EthanolHCID 66915691HCID 66915691, 화합물

생성물 1

HCID 1507363-O-Ethylascorbic acid수율 84.3%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 962Water용매

실험 절차

12.4 g of the 3-O-ethyl-isopropylidene ascorbic acid obtained in Example 1 was dissolved in 100 ml of distilled water, to which 10 ml of 2N hydrochloric acid solution was added. The mixture was reacted at 60° C. for 2 hours and concentrated under reduced pressure to give an adhesive liquid product. Ethanol was added to the prepared liquid product, which was then concentrated to give crude crystalline 3-ethyl-ascorbic acid. The crude crystalline 3-ethyl-ascorbic acid was re-crystallized in ethylacetate/ethanol (8:2) to give 8.6 g of white crystalline 3-O-ethyl-ascorbic acid (yield: 84.3%).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. additionwas added
  2. customThe mixture was reacted at 60° C. for 2 hours
  3. concentrationconcentrated under reduced pressure
  4. customto give an adhesive liquid product
  5. concentrationwas then concentrated
  6. customto give crude crystalline 3-ethyl-ascorbic acid
  7. customThe crude crystalline 3-ethyl-ascorbic acid was re-crystallized in ethylacetate/ethanol (8:2)

출처 및 근거

ORD 기록
ord-1dbce865394346f88324c9844697df1c
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07838690B2

반응 노트

불러오는 중…