Reaction #324409

ord-0689ebe28d7a446ca9a5361debad4212

Reaction equation

CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)O)cc1
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetic acid
O=C(Cl)C(=O)Cl
oxalyl dichloride
CC(C)(C)[Si](C)(C)Oc1ccc(CC(=O)Cl)cc1
2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherwhile elevating to room temperature
  2. 2
    ConcentrationThe mixture was concentrated under reduced pressure

Procedure

Under an argon atmosphere, to a solution of 2-[4-(tert-butyldimethylsilyloxy)phenyl]acetic acid (9) (170 mg, 638 μmol) in CH2Cl2 (5 mL) was added DMF (1 drop) by a Pasteur pipette at room temperature. To this was added oxalyl dichloride (110 μL, 1.30 mmol) at 0° C. and the mixture was stirred for 30 minutes while elevating to room temperature. The mixture was concentrated under reduced pressure to give crude 2-[4-(tert-butyldimethylsilyloxy)phenyl]acetyl chloride (10) as a colorless oil, which was used in the following reaction without further purification.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08642281B2uspto-grants-2014_02