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

Hydrochloric Acid → 12-Aminododecyl methanesulfonate hydrochloride

HRID 1003312
노트
인쇄 미리보기

반응식

HRID 1003312 반응식
[S:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH:18]C(=O)OC(C)(C)C)([CH3:4])(=[O:3])=[O:2].[ClH:26].CCCCCC>C(OCC)(=O)C>[ClH:26].[CH3:4][S:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][NH2:18])(=[O:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 8058HexaneHCID 18796422tert-butyl N-(12-mesyloxydodecyl)carbamate

생성물 1

HCID 1879641312-Aminododecyl methanesulfonate hydrochloride

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 8.06 g of tert-butyl N-(12-mesyloxydodecyl)carbamate in 60 ml of ethyl acetate was added 10 ml of hydrochloric acid under ice-cooling and the mixture was stirred at room temperature for one hour. The reaction solution was cooled with ice, hexane was added, the crystal thus precipitated out was recovered by filtration and dried under reduced pressure to afford the title compound.

후처리

  1. temperaturecooling
  2. additionwas added
  3. customthe crystal thus precipitated out
  4. filtrationwas recovered by filtration
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-f490ffdc90cf4417967bb689337bc940
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06046201

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트