تفاعل #5875

ord-e1764cad45a24269bfb95b0d00a282b2

معادلة التفاعل

CC1CC(=O)c2ccccc21
2,3-dihydro-3-methyl-1H-inden-1-one
COC(=O)CN
methyl 2-aminoacetate
c1ccsc1
thiophene
O=C[O-].[Na+]
sodium formate
CC1CC(N(C)CC(=O)O)c2ccccc21
methyl N-(2,3-dihydro-3-methyl-1H-inden-1-yl)glycine
المردود 54.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction mixture is evaporated
  2. 2
    workup.ADDITION1,1'-oxybisethane is added
  3. 3
    استخلاصThe separated organic layer is extracted with a hydrochloric acid solution 10%
  4. 4
    استخلاصthe product is extracted with 1,1'-oxybisethane
  5. 5
    أخرىThe combined extracts are dried
  6. 6
    ترشيحfiltered
  7. 7
    أخرىevaporated

الإجراء التجريبي

A mixture of 21 parts of 2,3-dihydro-3-methyl-1H-inden-1-one, 25 parts of methyl 2-aminoacetate, 2 parts of a solution of thiophene in methanol 4%, 25 parts of sodium formate and 480 parts of methanol is hydrogenated in a Parr-apparatus and at 50° C. with 5 parts of palladium-on-charcoal catalyst 10%. The reaction mixture is evaporated. The residue is taken up in water and 1,1'-oxybisethane is added. The separated organic layer is extracted with a hydrochloric acid solution 10%. The aqueous layer is made alkaline and the product is extracted with 1,1'-oxybisethane. The combined extracts are dried, filtered and evaporated, yielding 19 parts (54.1%) of methyl N-(2,3-dihydro-3-methyl-1H-inden-1-yl)glycine as a residue.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05246915uspto-grants-1993_09