HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → Boc-MePhe methioninol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | L-Methioninol | HCID 2724404 | — |
| Reactant | Boc-N-Me-Phe-OH | HCID 7010602 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-MePhe methioninol | HCID 131712176 | — |
Reaction Steps
3.1 g of Boc-MePhe-OH are dissolved in 30 ml of tetrahydrofuran, cooled to -20°, and 1.45 ml of N-ethylmorpholine are added with stirring followed by 1.45 ml of chloroformic acid iso-butyl ester and the mixture stirred for a further 5 minutes at -20°. A cold solution of 1.80 g of methioninol in 1 ml of tetrahydrofuran is added, the mixture left to stand for 2 hours at a temperature of from -5° to 0° and then stirred for 2 hours at room temperature. The reaction mixture is diluted with ca. 350 ml of acetic acid and washed repeatedly with water, 1 N citric acid, 10% KHCO3 and 30% NaCl solution. The organic phase is dried over Na2SO4 and evaporated, whereby Boc-MePhe-methioninol is obtained as an amorphous product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04261888 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-a177efbe882b49f99b0a5f2d55b737f4 |
| Source note | uspto-grants-1981_04 |