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

Sodium Hydroxide → (R)-2-((Benzyloxy)methyl)morpholine

HRID 2355426
노트
인쇄 미리보기

반응식

HRID 2355426 반응식
[CH2:1]([O:8][CH2:9][C@H:10]1[CH2:12][O:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].S(O)(O[CH2:19][CH2:20][NH2:21])(=O)=O>O.CO.C1(C)C=CC=CC=1>[CH2:1]([O:8][CH2:9][C@@H:10]1[O:11][CH2:19][CH2:20][NH:21][CH2:12]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 14798Sodium Hydroxide2회HCID 70223Aminoethyl sulfateHCID 159746(-)-Benzyl (R)-glycidyl ether

생성물 1

HCID 13670020(R)-2-((Benzyloxy)methyl)morpholine수율 110.9%

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매2회
HCID 1140Toluene용매2회

반응 조건

온도
40 °C

실험 절차

To a stirred mixture of (R)-2-(benzyloxymethyl)oxirane (10.0 g, 60.9 mmol) and NaOH (19.49 g, 487.2 mmol) in H2O (46 mL) and MeOH (18 mL), there was added 2-aminoethyl hydrogen sulfate (36.8 g, 255.8 mmol) in portions. After addition the reaction mixture was stirred at 40° C. for 2 h. After cooling, the mixture was treated with NaOH (15.0 g, 375.0 mmol) then toluene (70 mL) and stirred at 65° C. overnight. The mixture was cooled, diluted with toluene (27 mL) and H2O (92 mL). The toluene layer was separated and the aqueous layer was extracted with CH2Cl2 (2×50 mL). The combined organic layers were concentrated to give crude (R)-2-(benzyloxymethyl)morpholine (˜14 g), which was used without purification. MS m/z 208 (M+H+).

후처리

  1. additionAfter addition the reaction mixture
  2. temperatureAfter cooling
  3. temperatureThe mixture was cooled
  4. customThe toluene layer was separated
  5. extractionthe aqueous layer was extracted with CH2Cl2 (2×50 mL)
  6. concentrationThe combined organic layers were concentrated

출처 및 근거

ORD 기록
ord-209f0fb81d644ce9ab91dc830d3715ac
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07754737B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트