![61291-91-6](/CAS/GIF/61291-91-6.gif)
(4-METHYL-2-PHENYL-1,3-THIAZOL-5-YL)METHANOL synthesis
- Product Name:(4-METHYL-2-PHENYL-1,3-THIAZOL-5-YL)METHANOL
- CAS Number:61291-91-6
- Molecular formula:C11H11NOS
- Molecular Weight:205.28
![ETHYL 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLATE](/CAS/GIF/53715-64-3.gif)
53715-64-3
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![(4-METHYL-2-PHENYL-1,3-THIAZOL-5-YL)METHANOL](/CAS/GIF/61291-91-6.gif)
61291-91-6
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Yield:61291-91-6 85.1%
Reaction Conditions:
with lithium aluminium tetrahydride in tetrahydrofuran at 0; for 1.5 h;Inert atmosphere;
Steps:
3 [00129] Synthesis of 4-methyl-2-phenyl-5-thiazolemethanol (2a)
[00129] Synthesis of 4-methyl-2-phenyl-5-thiazolemethanol (2a) [00130] To a stirred solution of ethyl ester la (0.303 g, 1.237 mmol) in anhydrous THF (1 mL) at 0 °C was added 2M lithium aluminum hydride solution in THF (1.24 ml, 2.48 mmol). The resulting mixture was stirred under argon at 0 °C for 1.5 hours. The reaction mixture was quenched by the careful addition of 0.5 ml of water, followed by 2.5 ml of ethyl acetate and 0.92 g of anhydrous sodium sulfate. The mixture was stirred for 15 minutes and was filtered and concentrated under reduced pressure to give 2a as a light-yellow solid (0.215 g, 1.053 mmol, 85.1%). TLC Rf (25% EtOAc/Hexane) = 0.11. Mp 101-102 °C. FontWeight="Bold" FontSize="10" H NMR (CDC13, 600 MHz): δ ppm 7.88 (2H, d, J = 7.92 Hz), 7.41 (3H, m), 4.79 (2H, s), 2.94 (1H, s), 2.41 (3H, s).
References:
WO2014/152809,2014,A2 Location in patent:Paragraph 00129; 00130
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2227-79-4
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$6.00/5g
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61291-91-6
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![5-Thiazoleacetic acid, 4-methyl-2-phenyl-, ethyl ester](/CAS/20210305/GIF/111559-41-2.gif)
111559-41-2
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![(4-METHYL-2-PHENYL-1,3-THIAZOL-5-YL)METHANOL](/CAS/GIF/61291-91-6.gif)
61291-91-6
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$87.00/1g
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55-21-0
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$5.00/5G
![(4-METHYL-2-PHENYL-1,3-THIAZOL-5-YL)METHANOL](/CAS/GIF/61291-91-6.gif)
61291-91-6
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![4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBALDEHYDE](/CAS/GIF/55327-23-6.gif)
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![(4-METHYL-2-PHENYL-1,3-THIAZOL-5-YL)METHANOL](/CAS/GIF/61291-91-6.gif)
61291-91-6
30 suppliers
$87.00/1g