HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372994Generated: October 25, 2026
Benzylamine → 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranose
https://huagongshe.com/reaction/2372994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose | HCID 10991244 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranose | HCID 23240188 | 47.3% |
Reaction Steps
22 ml (0.2 mol) of benzylamine are added under an inert atmosphere to a solution of 15 g (44.8.10-3 mol) of 1,2,3,4-tetra-O-acetyl-5-thio-D-xylopyranose in 450 ml of ether. After 7 hours at room temperature (15°-25° C.), the reaction mixture is concentrated under reduced pressure and the residue is dissolved in methylene chloride and washed with a 1N solution of hydrochloric acid, a saturated solution of ammonium chloride and then water. The solution obtained is dried over sodium sulfate and the solvent is evaporated off under reduced pressure. 6.2 g (yield: 47%) of the expected product are obtained after purification by chromatography on silica gel using a hexane/ethyl acetate mixture (3/2 v/v) as the eluent, and crystallization from an ethyl acetate/hexane mixture, said product having the following physical characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05101048 |
|---|
| Source dataset | uspto-grants-1992_03 |
|---|
| ORD ID | ord-bd95c02756634ff68e5e92754f93bce0 |
|---|
| Source note | uspto-grants-1992_03 |
|---|