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Benzylethanolamine → 2-(Benzylamino)ethyl hydrogen sulfate

HRID 1864005
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HRID 1864005 반응식
Cl[S:2]([OH:5])(=[O:4])=[O:3].[C:6]1([CH2:12][NH:13][CH2:14][CH2:15][OH:16])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>C(Cl)(Cl)(Cl)Cl.C(Cl)(Cl)Cl.C(O)C>[S:2]([OH:5])([O:16][CH2:15][CH2:14][NH:13][CH2:12][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 4348BenzylethanolamineHCID 24638Chlorosulfonic acid

생성물 1

HCID 218250682-(Benzylamino)ethyl hydrogen sulfate수율 74%

시약·촉매·용매 3

HCID 702Ethanol용매HCID 5943Carbon Tetrachloride용매HCID 6212Chloroform용매

실험 절차

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Chlorosulfonic acid (13.3 mL, 0.2 mol) was added very slowly to (2-[(phenylmethyl)amino]ethanol (30.2 g, 0.2 mol) in carbon tetrachloride (100 mL) in an ice bath. The resulting thick white suspension was stirred at room temperature overnight The suspension was diluted with chloroform and ethanol, warmed to 45° C. and then cooled in an ice bath. The precipitate was collected by filtration, washed with ethanol and dried under vacuum for 16 hrs at 40° C. to afford the desired compound (34 g, 74%). MS (ES)+ m/z 232 [M+H]+.

후처리

  1. temperaturewarmed to 45° C.
  2. temperaturecooled in an ice bath
  3. filtrationThe precipitate was collected by filtration
  4. washwashed with ethanol
  5. customdried under vacuum for 16 hrs at 40° C.

출처 및 근거

ORD 기록
ord-ac5685c7b8084a4b95d5aebb6d9fb6d6
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07625890B2

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