تفاعل #1125

ord-db32eb67f898496ca933619d4788c566

معادلة التفاعل

OCC1CO1
2,3-epoxypropan-1-ol
[O-]c1ccccc1
phenoxide
CS(=O)(=O)OCC1CN(c2ccc(C#N)cc2)C(=O)O1
3-p-cyanophenyl-5-methanesulfonyloxymethyloxazolidin-2-one
N#Cc1ccc(N)cc1
p-aminobenzonitrile
N#Cc1ccc(NCC(O)CO)cc1
p-(N-2,3-dihydroxypropylamino)benzonitrile

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

1 Equivalent of NaH is added to a solution of 1.7 g of Na p-methoxycarbonylmethylphenoxide (obtainable by converting p-hydroxybenzyl cyanide into the corresponding carboxylic acid, esterifying with methanol to give p-methoxycarbonylmethylphenol and subsequently converting the latter into the phenoxide) in 20 ml of dimethylformamide (DMF), and the mixture is stirred at room temperature for 30 min. After that, 3.0 g of 3-p-cyanophenyl-5-methanesulfonyloxymethyloxazolidin-2-one ("A") (obtainable by reacting p-aminobenzonitrile with 2,3-epoxypropan-1-ol to give p-(N-2,3-dihydroxypropylamino)benzonitrile, reacting the latter with diethyl carbonate in the presence of K tert-butoxide to give 3-p-cyanophenyl-5-hydroxymethyloxazolidin-2-one and subsequently esterifying the latter with methanesulfone chloride), dissolved in 10 ml of DMF, are added and the mixture is once again stirred at room temperature for 15 min. Following removal of the solvent, and the customary working-up, 3-p-cyanophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one is obtained, M.p. 114°-115°.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723480uspto-grants-1998_03