تفاعل #324381

ord-09f51accf57e4502996e58fcbcabda73

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwhile elevating to room temperature
  2. 2
    تركيزThe mixture was concentrated under reduced pressure

الإجراء التجريبي

Under an argon atmosphere, to a mixture of 2-[4-(tert-butyldimethylsilyloxy)phenyl]acetic acid (9) (1.80 g, 6.76 mmol) in CH2Cl2 (15 mL) was added DMF (4 drops) by a Pasteur pipette at room temperature. To this was added oxalyl dichloride (1.20 mL, 14.2 mmol) at 0° C. and the mixture was stirred for an hour 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08642281B2uspto-grants-2014_02