تفاعل #40822

ord-f2ac45d32fa641e1bc045452d34d6cd4

معادلة التفاعل

CCOC(=O)c1ccc(-c2ccccc2)c(-c2ccccc2)n1
ethyl 5,6-diphenylpyridine-2-carboxylate
CCOC(=O)c1ccc(-c2ccccc2)c(-c2ccccc2)n1
Compound 21
CCOC(=O)c1ccc(-c2ccccc2)c(-c2ccccc2)n1
ethyl 5,6-diphenylpyridine-2-carboxylate
CC(C)[CH2][AlH][CH2]C(C)C
DIBAL-H
O=Cc1ccc(-c2ccccc2)c(-c2ccccc2)n1
title compound
O=Cc1ccc(-c2ccccc2)c(-c2ccccc2)n1
5,6-diphenylpyridine-2-carbaldehyde

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction was quenched with aq, NH4Cl, diethyl ether and 400 mg Celite
  2. 2
    workup.ADDITIONwere added
  3. 3
    workup.STIRRINGthe mixture was stirred at room temperature 30 min
  4. 4
    ترشيحThe solid was filtered off
  5. 5
    غسيلrinsed with ether
  6. 6
    تركيزthe combined filtrate was concentrated in vacuo
  7. 7
    أخرىthe residue was purified by column chromatography (silica gel, 15% ethyl acetate in hexane)

الإجراء التجريبي

General Procedure L. To a solution of ethyl 5,6-diphenylpyridine-2-carboxylate (Compound 21, 145 mg, 0.48 mmol) in CH2Cl2 (5 ml) at −78° C. was added DIBAL-H (0.72 ml, 0.72 mmol, 1.0 M in Toluene) and the mixture was stirred between −78° C. and −60° C. for 1 hour under argon. The reaction was quenched with aq, NH4Cl, diethyl ether and 400 mg Celite were added, and the mixture was stirred at room temperature 30 min. The solid was filtered off and rinsed with ether, and the combined filtrate was concentrated in vacuo, and the residue was purified by column chromatography (silica gel, 15% ethyl acetate in hexane) to produce the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07728014B2uspto-grants-2010_06