تفاعل #955979

ord-b056985c9b064ebcb89740d26e281de2

معادلة التفاعل

COCC1CCCN1N=C1CC(C)(C)C(O)(C=CC(C)=CCO)c2ccccc21
hydrazone alcohol
COCC1CCCN1N=C1CC(C)(C)C(O)(C=CC(C)=CCO)c2ccccc21
1-(5-Hydroxy-3-methyl-penta-1,3-dienyl)-4-(2-methoxymethyl-pyrrolidin-1-ylimino)-2,2-dimethyl-1,2,3,4-tetrahydro-naphthalen-1-ol
COCC1CCCN1N=C1CC(C)(C)C(O)(C=CC(C)=CC=O)c2ccccc21
hydrazone aldehyde
المردود 80.7%
COCC1CCCN1N=C1CC(C)(C)C(O)(C=CC(C)=CC=O)c2ccccc21
5-[1-Hydroxy-4-(2-methoxymethyl-pyrrolidin-1-ylimino)-2,2-dimethyl-1,2,3,4-tetrahydro-naphthalen-1-yl]-3-methyl-penta-2,4-dienal
المردود 80.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe reaction mixture was filtered over a bed of Celite®
  2. 2
    غسيلwashed with acetone
  3. 3
    أخرىThe combined filtrates and washings were evaporated
  4. 4
    أخرىto give a residue, which
  5. 5
    أخرىwas purified by column chromatography on silica using 30% ethyl acetate-hexane

الإجراء التجريبي

A mixture of hydrazone alcohol [29] (69 mg, 0.17 mmol) and MnO2 (300.8 mg, 3.46 mmol) in acetone (5 mL) was stirred at RT for 16 hr. The reaction mixture was filtered over a bed of Celite® and washed with acetone. The combined filtrates and washings were evaporated to give a residue, which was purified by column chromatography on silica using 30% ethyl acetate-hexane to provide the hydrazone aldehyde [30] (54.4 mg, 79%) and [α]D−532.6 (c 0.43, CH2Cl2).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08969249B2uspto-grants-2015_03