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Methanesulfonic Acid → HCID 20203369, 화합물

HRID 978630
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HRID 978630 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][S:5][CH2:4][CH2:3]1.[CH3:8][S:9]([OH:12])(=[O:11])=[O:10].[CH2:13]1[S:15][CH2:14]1>O>[CH3:8][S:9]([O-:12])(=[O:11])=[O:10].[CH3:1][N+:2]1([CH2:13][CH2:14][SH:15])[CH2:7][CH2:6][S:5][CH2:4][CH2:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6395Methanesulfonic AcidHCID 9865ThiiraneHCID 523249N-Methylthiomorpholine

생성물 1

HCID 20203369HCID 20203369, 화합물수율 86%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
65 °C

실험 절차

To precooled (ice bath) N-methylthiomorpholine* (5.00 g, 42.7 mmol) was added methanesulfonic acid (1.47 mL, 20.5 mmol) and ethylene sulfide (1.30 mL, 21.4 mmol). The mixture was heated at 65° C. for 24 h and diluted with water (25 mL). The aqueous solution was washed with diethyl ether (3×25 mL), pumped under vacuum and poured over a silica gel reverse phase column; the title compound being eluted with water. The appropriate fractions were combined and evaporated to afford the thiol as an oil (4.80 g, yield 86%); ir (film) νmax : 2550 cm-1 (w, SH); 1Hmr (DMSO d6)δ: 3.25-2.95 (6H, m, CH2N⊕), 3,32 (3H, s, CH3N⊕), 3.20-2.65 (7H, m, CH2S, SH) and 2.32 ppm (3H, s, CH3SO3).

후처리

  1. washThe aqueous solution was washed with diethyl ether (3×25 mL)
  2. additionpoured over a silica gel reverse phase column
  3. washthe title compound being eluted with water
  4. customevaporated

출처 및 근거

ORD 기록
ord-b39076dbb62e4e2ea5ea486394d9b237
출처 데이터셋
uspto-grants-1987_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04665170

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