Phenetole → (5-Bromo-2-chloro-3-methoxyphenyl)(4-ethoxyphenyl)methanone

To a solution of acid 56 (4.9 g, 18.57 mmol) in CH2Cl2 (62 mL) were added oxalyl chloride (2.1 mL, 24.14 mmol) and catalytic amounts of DMF at room temperature. The mixture was stirred at room temperature for 3 hours. The mixture was evaporated in vacuo and dried under high vacuum. The crude acid chloride was dissolved with CH2Cl2 (93 mL) and cooled to 0° C. To the mixture was added phenetole (2.4 mL, 18.57 mmol) at 0° C. and stirred at 0° C. for 5 min. To the reaction mixture was added AlCl3 (2.7 g, 20.43 mmol) portionwise at 0° C. The mixture was stirred at 0° C. for 30 min, warmed up to room temperature and stirred at room temperature for 15 hours. The mixture was poured into ice-water and extracted with CH2Cl2 (100 mL×2). The combined organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The crude product 73 was dried under high vacuum and used without further purification (7.0 g).

1. customThe mixture was evaporated in vacuo
2. customdried under high vacuum
3. dissolutionThe crude acid chloride was dissolved with CH2Cl2 (93 mL)
4. temperaturecooled to 0° C
5. stirringstirred at 0° C. for 5 min
6. stirringThe mixture was stirred at 0° C. for 30 min
7. temperaturewarmed up to room temperature
8. stirringstirred at room temperature for 15 hours
9. extractionextracted with CH2Cl2 (100 mL×2)
10. dry with materialThe combined organic layer was dried over MgSO4
11. filtrationfiltered
12. concentrationconcentrated in vacuo
13. dry with materialThe crude product 73 was dried under high vacuum
14. customused without further purification (7.0 g)

ORDレコード

ord-b2b7fc3b24c249028b4d40061bc7c671

出典データセット

uspto-grants-2015_05

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09034921B2