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

Water → HCID 21961225, 화합물

HRID 1445325
노트
인쇄 미리보기

반응식

HRID 1445325 반응식
[OH:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1[C:7]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=1)=[O:8].C([O:20][CH2:21][CH:22]1[CH:27]([O:28]C(=O)C)[CH:26]([O:32]C(=O)C)[CH:25]([O:36]C(=O)C)[CH:24](Br)[O:23]1)(=O)C.C(=O)([O-])[O-].[K+].[K+].O>ClCCl.[Cl-].C([N+](CCCC)(CCCC)CCCC)C1C=CC=CC=1>[CH3:16][O:15][C:12]1[CH:13]=[CH:14][C:9]([C:7]([C:3]2[S:4][CH:5]=[CH:6][C:2]=2[O:1][CH:24]2[CH:25]([OH:36])[CH:26]([OH:32])[CH:27]([OH:28])[CH:22]([CH2:21][OH:20])[O:23]2)=[O:8])=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 102932alpha-D-Galactopyranosyl bromide, tetraacetateHCID 135744175647833-71-4

생성물 1

HCID 21961225HCID 21961225, 화합물

시약·촉매·용매 2

HCID 159952Benzyltributylammonium chloride촉매
HCID 6344
Dichloromethane
용매

실험 절차

2.8 g of (3-hydroxythiophen-2-yl)-(4-methoxy-phenyl)-methanone were dissolved in 350 ml of dichloromethane, and 12.64 g of 3,4,5-triacetoxy-6-bromo-tetrahydropyran-2-ylmethyl actate, 15.4 g of potassium carbonate, 3.6 g of benzyltributylamonium chloride and finally 3 ml of water were added. The mixture was vigorously stirred at room temp. for 20 h. After the reaction was complete, the residue after filtration and concentration was filtered through SiO2 with ethyl acetate/heptane'1:2. The solvent was removed and the residue was taken up in about 300 ml of methanol and, after addition of 35 ml of 1 N NaOCH3 solution in methanol, stirred at room temp. for 1 h. This was followed by neutralization with 7% methanolic hydrochloric acid (about 35 ml), addition of about 100 of dichloromethane/methanol/conc. ammonia=30:5:0.1 mobile phase mixture and stirring for 5 min. This was followed by concentration, taking up the residue with the same mobile phase mixture and removing insoluble salt from the solution. Chromatography on silica gel results in the product with the molecular weight of 396.42 (C18H20O8S), MS (ESI): 397 (M+H+), 235 (M+H+-gluc).

후처리

  1. filtrationthe residue after filtration and concentration
  2. filtrationwas filtered through SiO2 with ethyl acetate/heptane'1
  3. customThe solvent was removed
  4. additionafter addition of 35 ml of 1 N NaOCH3 solution in methanol
  5. stirringstirred at room temp. for 1 h
  6. additionThis was followed by neutralization with 7% methanolic hydrochloric acid (about 35 ml), addition of about 100 of dichloromethane/methanol/conc
  7. stirringammonia=30:5:0.1 mobile phase mixture and stirring for 5 min
  8. concentrationThis was followed by concentration
  9. customremoving insoluble salt from the solution
  10. customChromatography on silica gel results in the product with the molecular weight of 396.42 (C18H20O8S), MS (ESI)

출처 및 근거

ORD 기록
ord-aa9452915c574e41b3f80a01e7406481
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07666848B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트