Triethylamine → HCID 67302267, compound

Temperature

-35 °C

A solution of 6.1 g (19.0 mmol) (1R)-B-chlorodiisopinocampheylborane in 40 mL THF was added dropwise within 30 min to a solution of 5.1 g (15.8 mmol) 3-(3,4-dibromo-phenyl)-2-oxo-propionic acid and 2.2 mL (15.8 mmol) triethylamine in 20 mL THF which had been cooled to −35° C. and the reaction mixture was kept at this temperature for 1 h. The reaction solution was carefully combined with 30 mL 1 M NaOH (exothermic) and 30 mL tert-butylmethylether, stirred for 15 min, the organic phase was separated off, then extracted with 25 mL water and 15 mL 1 M NaOH. The combined aqueous phases were acidified with 2 M HCl, extracted three times with in each case 40 mL tert-butylmethylether and the combined organic phases were dried over Na2SO4. After the desiccant and solvent had been eliminated the residue was purified by chromatography (silica gel, EtOAc/MeOH/NH3 70:30:3).

1. customthe organic phase was separated off
2. extractionextracted with 25 mL water and 15 mL 1 M NaOH
3. extractionextracted three times with in each case 40 mL tert-butylmethylether
4. dry with materialthe combined organic phases were dried over Na2SO4
5. customwas purified by chromatography (silica gel, EtOAc/MeOH/NH3 70:30:3)

ORD record

ord-b6fec8b0f2734931948768e6232b6a28

Source dataset

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07696196B2