HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 22827923, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | HCID 22827924 | HCID 22827924 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22827923 | HCID 22827923 | — |
Reaction Steps
To 0.200 ml of diisopropylamine was added to 0.426 g of 4-nitrobenzyl 6(S)-[1(R)-hydroxyethyl]-7-oxo-3-thioxo-4-thia-1-azabicyclo[3,2,0]heptane-2-carboxylate in dry tetrahydrofuran with stirring. 0.252 ml of iodoethane was then added and stirring was continued for 16 hours at room temperature. The reaction mixture was then evaporated to dryness and chromatographed on silica gel, eluting with ethyl acetate/hexane mixtures, to give the title product as a mixture of 5R and 5S isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04510086 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-dfe7832a5a0649e0b6b7b6c05041ed45 |
| Source note | uspto-grants-1985_04 |