HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[(R)-1-ethoxycarbonyl-2-heptylthioethyl]-alanine t-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl 2-bromopropanoate | HCID 545327 | — |
| Reactant | S-heptyl-L-cysteine ethyl ester | HCID 13647885 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | N-[(R)-1-ethoxycarbonyl-2-heptylthioethyl]-alanine t-butyl ester | HCID 13647889 | — |
Reaction Steps
In 20 ml of HMPA were dissolved 5.9 g of S-heptyl-L-cysteine ethyl ester and 5.5 g of 2-bromopropionic acid t-butyl ester. A 3.4 ml quantity of triethylamine was added to the solution. The mixture was stirred at room temperature for 24 hours. The reaction mixture was poured into ice water, followed by extraction with ethyl acetate. The extract was sufficiently washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the residue was separated and purified by silica gel column chromatography (a 1:3 mixture of ether and n-hexane as an eluent), producing the α-isomer of the title compound as a colorless oil from the first eluate. Yield 2.8 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04886813 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-38a6d986becf47b1ae07f3b35b88d9d0 |
| Source note | uspto-grants-1989_12 |