2,2,2-Cryptand → HCID 58518875, 화합물

HRID 217555

반응식

HRID 217555 반응식
[F-:1].[K+].C1N2CCOCCOCCN(CCOCCOCC2)CCOCCOC1.Cl[CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=1[S:37][CH2:38][CH2:39][CH:40]1[O:44][CH2:43][CH2:42][O:41]1>C(#N)C>[F:1][CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=1[S:37][CH2:38][CH2:39][CH:40]1[O:44][CH2:43][CH2:42][O:41]1

참가 물질

5

실험 절차

Potassium fluoride (3.5 mg, 0.060 mmol) and kryptofix 222 (22.5 mg, 0.060 mmol) were dissolved in acetonitrile (1 ml) and added to 2-[2-(2-chloromethyl-phenylsulfanyl)-ethyl]-[1,3]dioxolane (7.7 mg, 0.030 mmol) in acetonitrile (1 ml). The reaction mixture was heated to 70 degrees for 30 minutes. The crude product was purified by reverse phase preparative chromatography (Vydac 218TP1022 column; solvents A=water/0.1% TFA and B=CH3CN/0.1% TFA; gradient 40-80% B over 40 min; flow 10 ml/minute; detection at 254 nm). The fractions were left in the fridge overnight and to the acetonitrile phase was added diethyl ether, dried (Na2SO4) and evaporated under reduced pressure. (Analytical HPLC: Vydac 218TP54 column; solvents: A=water/0.1% TFA and B=CH3CN/0.1% TFA; gradient 40-80% B over 20 min; flow 1.0 ml/minute; retention time 9.200 minutes detected at 214 and 254 nm). Structure verified by NMR.

후처리

  1. temperatureThe reaction mixture was heated to 70 degrees for 30 minutes
  2. customThe crude product was purified by reverse phase preparative chromatography (Vydac 218TP1022 column; solvents A=water/0.1% TFA and B=CH3CN/0.1% TFA; gradient 40-80% B over 40 min; flow 10 ml/minute; detection at 254 nm)
  3. additionwas added diethyl ether
  4. dry with materialdried (Na2SO4)
  5. customevaporated under reduced pressure
  6. waitgradient 40-80% B over 20 min

출처 및 근거

ORD 기록
ord-35735f1d33d54c8ab1e2ca5bd46efe7c
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08197793B2

연결된 노트

불러오는 중…