تفاعل #1876806

ord-b8c3fe7d8c714fd3a9fe2ffe54494878

معادلة التفاعل

O.[Li+].[OH-]
lithium hydroxide monohydrate
CCOCOc1ccc(NC(=O)OC(C)(C)C)cc1C=CC(=O)OC
methyl 3-(5-tert.butoxycarbonylamino-2-ethoxymethoxyphenyl)acrylate
O=P([O-])([O-])[O-]
phosphate
CCOCOc1ccc(NC(=O)OC(C)(C)C)cc1C=CC(=O)O
3-(5-tert.butoxycarbonylamino-2-ethoxymethoxyphenyl)acrylic acid

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate
  2. 2
    غسيلthe organic phase was washed with a saturated aqueous sodium chloride solution
  3. 3
    تجفيفdried over sodium sulfate
  4. 4
    أخرىThe organic phase was partially evaporated to incipient formation of a precipitate, and hexane
  5. 5
    workup.ADDITIONwas then added
  6. 6
    ترشيحThe precipitate was filtered off
  7. 7
    غسيلwashed with 50 mL of hexane

الإجراء التجريبي

2.53 g (0.06 mol) of lithium hydroxide monohydrate was added at 0° C. to a solution of 6.3 g (0.018 mol) of methyl 3-(5-tert.butoxycarbonylamino-2-ethoxymethoxyphenyl)acrylate from step D in 50 mL of tetrahydrofuran, 15 mL of methanol and 30 mL of water. The mixture was allowed to agitate 24 hours at 60° C. The reaction mixture was then poured onto a phosphate buffer solution (pH 7.0) and extracted with ethyl acetate, and the organic phase was washed with a saturated aqueous sodium chloride solution and then dried over sodium sulfate. The organic phase was partially evaporated to incipient formation of a precipitate, and hexane was then added. The precipitate was filtered off and washed with 50 mL of hexane. This gave 5.4 g (89% of the theoretical) of 3-(5-tert.butoxycarbonylamino-2-ethoxymethoxyphenyl)acrylic acid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07070626B2uspto-grants-2006_07