HuagongsheHuagongshe Chemistry Print Report · For research reference only
s-Glycerylcysteine → N-Fluorenylmethoxycarbonyl-S-(2,3-dihydroxypropyl)cysteine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | s-Glycerylcysteine | HCID 15060047 | — |
| Reactant | fluorenylmethoxycarbonyl-N-hydroxysuccinimide | HCID 21219419 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | N-Fluorenylmethoxycarbonyl-S-(2,3-dihydroxypropyl)cysteine | HCID 66831030 | 63.8% |
Reaction Steps
S-(2,3-dihydroxypropyl)cysteine (2.45 g, 12.6 mmole) was dissolved in 9% sodium carbonate (20 ml). A solution of fluorenylmethoxycarbonyl-N-hydroxysuccinimide (3.45 g, 10.5 mmole) in acetonitrile (20 ml) was added and the mixture stirred for 2 h, then diluted with water (240 ml), and extracted with diethyl ether (25 ml×3). The aqueous phase was acidified to pH 2 with concentrated hydrochloric acid and was then extracted with ethyl acetate (70 ml×3). The extract was washed with water (50 ml×2) and saturated sodium chloride solution (50 ml×2), dried over sodium sulfate and evaporated to dryness. Recrystalisation from ether and ethyl acetate at −20° C. yielded a colourless powder (2.8 g, 6.7 mmole, 63.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07833532B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-c58f9ee41d3d4c2a8d9755443e743e53 |
| Source note | uspto-grants-2010_11 |