HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → methyl N-t-butoxycarbonyl-S-[(3,4-methylenedioxy)phenyl]cysteinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,4-(Methylenedioxy)thiophenol | HCID 2759847 | — |
| Reactant | Boc-Ser(Tos)-OMe | HCID 7009424 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | methyl N-t-butoxycarbonyl-S-[(3,4-methylenedioxy)phenyl]cysteinate | HCID 18652697 | 66% |
Reaction Steps
After 27.7 g of (3,4-methylenedioxy)thiophenol and 74 g of methyl N-(t-butoxycarbonyl)-O-tosyl-L-serinate were dissolved in 200 ml of chloroform, 20 g of triethylamine were added at room temperature, followed by stirring overnight. The reaction mixture was washed with water and then extracted with ethyl acetate. The extract so obtained was dried over anhydrous magnesium sulfate. After the solvent was distilled off, 49 g of crude oil were obtained. The crude oil was recrystallized from an ethyl acetatehexane system, whereby 42 g of methyl N-t-butoxycarbonyl-S-[(3,4-methylenedioxy)phenyl]cysteinate were obtained (yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05227398 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-b7ea69842239425ca8143b0c5d4aa26f |
| Source note | uspto-grants-1993_07 |