Triethylamine → HCID 59476871、化合物

温度

0 °C

To a 200-mL three-necked flask fitted with a stirrer bar coated with Teflon™, were added 5.95 g of 4-hydroxy-4-methyltetrahydrothiopyran (manufactured by SANKYO KASEI Co., Ltd.), 5.08 g of triethyl amine, and 50 mL of dried methylene chloride, and the mixture was stirred under nitrogen atmosphere at 0° C. To the mixture, 5.0 g of methacryloyl chloride was slowly added through a dropping funnel, and the resulted mixture was reacted at 0° C. for 30 minutes, allowed to warm to room temperature, and was further reacted for another 5 hours. After confirming loss of the starting material by TLC, the reaction solution was poured in a 300-mL separatory funnel, washed with 100 mL of water followed by with 100 mL of saturated NaCl solution (brine), and dried with anhydrous sodium sulfate. From the obtained solution, the solvent was removed by an evaporator, to obtain an oily crude product. The crude product was purified by silica gel chromatography using a mixed solution of n-hexane and ethyl acetate to give 5.89 g of 4-methyl-tetrahydro-2H-thiopyran-4-yl methacrylate (thiopyran derivative of the following formula 3) (yield: 59.4%).

1. customTo a 200-mL three-necked flask fitted with a stirrer bar
2. customthe resulted mixture was reacted at 0° C. for 30 minutes
3. temperatureto warm to room temperature
4. customwas further reacted for another 5 hours
5. additionthe reaction solution was poured in a 300-mL separatory funnel
6. washwashed with 100 mL of water
7. dry with materialdried with anhydrous sodium sulfate
8. customFrom the obtained solution, the solvent was removed by an evaporator
9. customto obtain an oily crude product
10. customThe crude product was purified by silica gel chromatography

ORDレコード

ord-60cb84fb949d4db8ae677088431bc872

出典データセット

uspto-grants-2011_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08080365B2