Triethylamine → HCID 67301744, compound

Temperature

-35 °C

Under a nitrogen atmosphere a mixture of 2.6 g (12.23 mmol) 3-(3-chloro-4-methyl-phenyl)-2-oxo-propionic acid and 2.1 mL (15.1 mmol) triethylamine in 40 mL THF was cooled to −35° C. Then a solution of 5.87 g (18.30 mmol) (1R)-B-chlorodiisopinocampheylborane in 20 mL THF was added dropwise so that the reaction temperature remained between −35° C. and −25° C. The cooling bath was removed and the reaction mixture was stirred overnight at RT. While cooling with ice 30 mL 1 M NaOH and 60 mL diethyl ether were added dropwise and the mixture was stirred for 15 min. The aqueous phase was separated off, the organic phase was extracted twice with 20 mL 1 M NaOH and once with 20 mL water. The combined aqueous phases were acidified with semiconc. HCl while cooling with ice, extracted twice with 60 mL EtOAc and the combined organic phases were dried over Na2SO4. After the desiccant and solvent had been eliminated the residue was reacted further without purification.

1. customremained between −35° C. and −25° C
2. customThe cooling bath was removed
3. temperatureWhile cooling with ice 30 mL 1 M NaOH and 60 mL diethyl ether
4. additionwere added dropwise
5. stirringthe mixture was stirred for 15 min
6. customThe aqueous phase was separated off
7. extractionthe organic phase was extracted twice with 20 mL 1 M NaOH and once with 20 mL water
8. temperatureHCl while cooling with ice
9. extractionextracted twice with 60 mL EtOAc
10. dry with materialthe combined organic phases were dried over Na2SO4
11. customwas reacted further without purification

ORD record

ord-14bc07dabd454ed0a7891a32b17812f1

Source dataset

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07696196B2