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

Water → 2,3,5-Triiodobenzyl mesylate

HRID 58354
노트
인쇄 미리보기

반응식

HRID 58354 반응식
[S:1](Cl)([CH3:4])(=[O:3])=[O:2].[I:6][C:7]1[C:14]([I:15])=[CH:13][C:12]([I:16])=[CH:11][C:8]=1[CH2:9][OH:10].C(N(C(C)C)CC)(C)C.O>ClCCl>[S:1]([O:10][CH2:9][C:8]1[CH:11]=[C:12]([I:16])[CH:13]=[C:14]([I:15])[C:7]=1[I:6])(=[O:3])(=[O:2])[CH3:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 31297Methanesulfonyl chlorideHCID 81531DiisopropylethylamineHCID 34957432,3,5-Triiodobenzyl alcohol

생성물 1

HCID 866822052,3,5-Triiodobenzyl mesylate수율 84%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

Mesyl chloride (0.6 ml, 8 mmol) was added dropwise to a suspension of 2,3,5-triiodobenzyl alcohol 1 (1.94 g, 4 mmol) in dry dichloromethane (30 ml) containing diisopropylethylamine (1.4 ml, 8 mmol) at 0° C. under dry nitrogen gas flow. The reaction mixture was stirred 1 h15 at 0° C., then cold H2O (40 ml) was added. The resulting aqueous phase was extracted with dichloromethane (10 ml). The combined organic extracts were washed with H2O (8 ml) then dried (Na2SO4), filtered and concentrated. The pale yellow solid was also washed with cold methanol (35 ml). 1.894 g of 2,3,5-triiodobenzyl mesylate in the form of a white clean solid was obtained in 84% yield.

후처리

  1. extractionThe resulting aqueous phase was extracted with dichloromethane (10 ml)
  2. washThe combined organic extracts were washed with H2O (8 ml)
  3. dry with materialthen dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. washThe pale yellow solid was also washed with cold methanol (35 ml)

출처 및 근거

ORD 기록
ord-06f0003fb7f04460a0642a8020f29f7e
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434800B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트