Diisopropylamine → HCID 178469142, compound

Temperature

10 °C

To a -78° C. solution of LDA (0.10 mol), prepared from 0.10 mol of n-BuLi and 14 ml (0.10 mol) of diisopropylamine in 70 ml ether was added a solution of 10.0 g (0.042 mol) of product of Example 34 in 20 ml of ether slowly to maintain a temperature below -60° C. After stirring for 30 minutes, the reaction mixture was treated with 21 ml (0.042 mol) of ethyl pentafluoropropionate. After stirring at -78° C. for 15 minutes, the reaction mixture was warmed to 10° C. in 0.5 hour and poured into 100 ml of water, and extracted with ether. The ether extract was extracted with 10% K2CO3. The combined aqueous layer and K2CO3 extract was acidified with concentrated HCl to give 4.73 g (29.5%) of beige solid; mp 115°-117° C. (dec). A 2.73 g (0.00709 mol) of the solid was heated in a kugelrohr pot at 130° C. for 0.5 hour. The distillate and residue were combined and dissolved in ether. The ether solution was dried (CaSO4) and concentrated to give 2.0 g (76.9%) of product as a solid; mp 36°-38° C.

1. temperatureto maintain a temperature below -60° C
2. stirringAfter stirring at -78° C. for 15 minutes
3. extractionextracted with ether
4. extractionThe ether extract
5. extractionwas extracted with 10% K2CO3
6. extractionThe combined aqueous layer and K2CO3 extract

ORD record

ord-b132052dda1a42b084f6d6e2749934bd

Source dataset

uspto-grants-1987_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04655816