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Potassium Carbonate → 6-(4-Methylthiazol-2-yl)thiohexan-1-ol

HRID 892748
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HRID 892748 반응식
[SH:1][C:2]1[S:3][CH:4]=[C:5]([CH3:7])[N:6]=1.Br[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][OH:15].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH3:7][C:5]1[N:6]=[C:2]([S:1][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][OH:15])[S:3][CH:4]=1
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 779706-Bromo-1-hexanolHCID 1784319804-methyl-1,3-thiazole-2-thiol

생성물 1

HCID 198940506-(4-Methylthiazol-2-yl)thiohexan-1-ol수율 99%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

The mixture of 2-mercapto-4-methylthiazole (2.62 g, 0.02 mol), 6-bromo-1-hexanol (3.62 g, 0.02 mol), potassium carbonate (2.76 g, 0.02 mol) and acetone (50 mL) was refluxed for 14 h. After cooling, the mixture was filtered and the filtrate was evaporated. The residual oil was purified by elution from a silica gel column using ethylacetate-methanol (99:1, v./v) as eluant to give 6-(4-methylthiazol-2-yl)thiohexan-1-ol (29) (99%) as a yellowish oil. IR (neat) 3608 (OH)cm-1 ; NMR (CDCl3) 1.25-2.10 (m, 8H, (CH2)4), 2.38 (S, 3H, Me-Het), 3.18 (t, J=9 Hz, 2H, CH2 --S), 3 65 (t, J=9 Hz, 2H, CH2 --O), 6.75 (S, 1H, H-Het). Analysis found: C, 51.98; H, 7.49; N, 5.92; S, 27.65. Required: C, 51.90; H, 7.40; N, 6.08; S, 27.71 (C10H17NOS2). ##STR11##

후처리

  1. temperaturewas refluxed for 14 h
  2. temperatureAfter cooling
  3. filtrationthe mixture was filtered
  4. customthe filtrate was evaporated
  5. customThe residual oil was purified by elution from a silica gel column

출처 및 근거

ORD 기록
ord-0a2ea6b803a6411c9ace19630ff7d4c5
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05120750

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