4-Chlorophenol → 2-Chloro-1-(5-chloro-2-hydroxyphenyl)ethanone

Temperature

80 °C

(Ref: J. Org. Chem. 1955; 20; 813-818) A mixture of 4-chlorophenol (5 g; 39.0 mmol) and chloroacetyl chloride (3.41 mL; 42.8 mmol) was heated to 80° C. for 2.5 hours. Mixture cooled to 30° C. and aluminum chloride (5.2 g; 39.0 mmol) was added over 30 minutes. Mixture heated to 130° C. for 15 hours. Mixture cooled under N2 flow and reaction was quenched with 0.5 g of ice chuncks over 5 minutes. Mixture was treated with 12 mLs of 20% HCl and heated to 60° C. for 15 minutes (fumes generated). Mixture cooled back room temperature and after 30 minutes 2 phases observed. Aqueous phase was extracted, and oil organic layer was triturated with petroleum ether. Petroleum ether was decanted off. Mixture was then heated to 60° C. in 100 mL of benzene and charcoal. Mixture filtered and filtrate was concentrated to a third volume. Another 40 mLs of petroleum ether added and allowed to stand overnight. Mixture was decanted and mother liquor was evaporated to afford 2-chloro-1-(5-chloro-2-hydroxy-phenyl)-ethanone. (5 g; 63% yield).

1. temperatureMixture cooled to 30° C.
2. temperatureMixture heated to 130° C. for 15 hours
3. temperatureMixture cooled under N2
4. customflow and reaction
5. customwas quenched with 0.5 g of ice chuncks over 5 minutes
6. additionMixture was treated with 12 mLs of 20% HCl
7. temperatureheated to 60° C. for 15 minutes (fumes generated)
8. temperatureMixture cooled back room temperature and after 30 minutes 2 phases
9. extractionAqueous phase was extracted
10. customoil organic layer was triturated with petroleum ether
11. customPetroleum ether was decanted off
12. temperatureMixture was then heated to 60° C. in 100 mL of benzene
13. filtrationMixture filtered
14. concentrationfiltrate was concentrated to a third volume
15. additionAnother 40 mLs of petroleum ether added
16. customMixture was decanted
17. custommother liquor was evaporated

ORD record

ord-31c881d7c97f4a6cbc489f6beac40f80

Source dataset

uspto-grants-2015_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09067897B2