Acetone → HCID 53959320, compound

To a solution of 4-nitrocinnamaldehyde 8 (110 mg, 0.61 mmol; alternatively other aldehyde acceptors are shown in the Figures and can be obtained commercially or as described herein) in 15 mL of DMF and 31 mL of acetone (alternatively other ketone donors are shown in the Figures and can be obtained commercially or as described herein), PBS buffer (571 mL, degassed and kept under argon) was added slowly to avoid precipitation. Antibody 38C2 (8.0 mL of a 120 mM solution) was added. The final concentrations of 4-nitrocinnamaldehyde and Ab38C2 were 1.0 mM and 1.9 mM, respectively in a total volume of 625 mL containing 5% (v/v) of acetone. The reaction mixture was kept in a dark place at room temperature for seven days under Argon. The reaction mixture was saturated with sodium chloride and extracted with 3×150 mL of ethyl acetate. The extracts were dried over MgSO4 and evaporated to yield 140 mg of crude product. Purification by FC (1:2, ethyl acetate/hexane) gave 96 mg (67%) of pure aldol product (30) with an ee of 91%.

1. customcan be obtained commercially
2. customcan be obtained commercially
3. customPBS buffer (571 mL, degassed and kept under argon)
4. additionwas added slowly
5. customprecipitation
6. additionAntibody 38C2 (8.0 mL of a 120 mM solution) was added
7. additionrespectively in a total volume of 625 mL containing 5% (v/v) of acetone
8. extractionextracted with 3×150 mL of ethyl acetate
9. dry with materialThe extracts were dried over MgSO4
10. customevaporated
11. customto yield 140 mg of crude product
12. customPurification by FC (1:2, ethyl acetate/hexane)

ORD record

ord-89ecacee868a49b08a522fda28b5d7ad

Source dataset

uspto-grants-2001_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06326176B1