1-(4-T-Butylphenyl)-3-chloropropan-1-one → 5-Tert-butyl-2,3-dihydroinden-1-one

温度

100 °C

1-(4-tert-Butyl-phenyl)-3-chloro-propan-1-one (45.6 g, 447 mmol) was taken up in concentrated sulfuric acid (200 mL) and the resulting mixture was heated to 100° C. with stirring for 2.5 hours. TLC indicated that all of the starting material had been consumed. After cooling to room temperature, the reaction mixture was very carefully poured onto about 1 Kg of crushed ice. Then some diethyl ether was added and the mixture was stirred carefully until it had cooled to about room temperature. Ethyl acetate (1200 mL) was added and after partitioning, the layers were separated. The acidic layer was then further extracted with ethyl acetate (2×200 mL). The combined ethyl acetate layers were washed with saturated sodium bicarbonate (5×300 mL). Finally the ethyl acetate layer was dried over magnesium sulfate, filtered, concentrated and pumped to dryness to afford the title compound as a colorless oil (15.764 g).

1. customhad been consumed
2. temperatureAfter cooling to room temperature
3. additionthe reaction mixture was very carefully poured onto about 1 Kg of crushed ice
4. additionThen some diethyl ether was added
5. stirringthe mixture was stirred carefully until it
6. temperaturehad cooled to about room temperature
7. additionEthyl acetate (1200 mL) was added
8. customafter partitioning
9. customthe layers were separated
10. extractionThe acidic layer was then further extracted with ethyl acetate (2×200 mL)
11. washThe combined ethyl acetate layers were washed with saturated sodium bicarbonate (5×300 mL)
12. dry with materialFinally the ethyl acetate layer was dried over magnesium sulfate
13. filtrationfiltered
14. concentrationconcentrated

ORDレコード

ord-28d0bbf7e61c4a448d50f9f325b628b2

出典データセット

uspto-grants-2013_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08536166B2