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

Potassium Carbonate → Tert-butyl 1,1-dioxo-1lambda6,2,6-thiadiazinane-2-carboxylate

HRID 1522056
노트
인쇄 미리보기

반응식

HRID 1522056 반응식
Cl[CH2:2][CH2:3][CH2:4][NH:5][S:6]([NH:9][C:10](=[O:16])[O:11][C:12]([CH3:15])([CH3:14])[CH3:13])(=[O:8])=[O:7].C([O-])([O-])=O.[K+].[K+]>CS(C)=O>[S:6]1(=[O:8])(=[O:7])[NH:5][CH2:4][CH2:3][CH2:2][N:9]1[C:10]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 23584604HCID 23584604, 화합물

생성물 1

HCID 23583903Tert-butyl 1,1-dioxo-1lambda6,2,6-thiadiazinane-2-carboxylate수율 40%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

To a solution of tert-butyl N-(3-chloropropyl)sulfamoylcarbamate (2 g, 7.333 mmol) in DMSO (10 mL), was added K2CO3 (5.068 g, 36.665 mmol) at room temperature. The reaction mixture was agitated for 4 hr and extracted using ethyl acetate and NH4Cl solution. The organic layer was dried over MgSO4. The residue was purified by silica gel column chromatography to give tert-butyl 1,2,6-thiadiazinan-2-carboxylate 1,1-dioxide (689 mg, 2.92 mmol, 40%, white solid). 1H NMR (300 MHz, CDCl3): δ 4.47 (br, 1H), 3.95-3.91 (m, 2H), 3.55-3.49 (m, 2H), 1.89-1.82 (m, 2H), 1.54 (m, 9H).

후처리

  1. extractionextracted
  2. dry with materialThe organic layer was dried over MgSO4
  3. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-c4b6b1ef80924fce92eb1f022df06b9f
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073906B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트