HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → methyl N-(tert-butoxycarbonyl)glycylglycinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycine methyl ester hydrochloride | HCID 122755 | — |
| Reactant | t-Butoxycarbonylglycine-2,4,5-Trichlorophenyl Ester | HCID 12799284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl N-(tert-butoxycarbonyl)glycylglycinate | HCID 637608 | — |
Reaction Steps
Prepare a solution of 1.98 g. of glycine methyl ester hydrochloride in dimethylformamide containing 8 ml. of methanol and 1.42 g. of triethylamine. Cool and stir the solution while adding 5.0 g. of t-butoxycarbonylglycine-2,4,5-trichlorophenyl ester in 25 ml. of dimethylformamide. Stir the reaction mixture overnight, filter and evaporate the filtrate to dryness under reduced pressure. Chromatograph the residue on 150 g. of silica gel and collect the desired product which is eluted by an ethyl acetate:chloroform (1:9) mixture. Evaporate the eluate to dryness and crystallize from hexane to obtain the title product (m.p. 132°-135° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04169141 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-442fb92c95e24a1fa5e17d9ac1377c25 |
| Source note | uspto-grants-1979_09 |