HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloroacetonitrile → 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranosyl trichloroacetimidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranose | HCID 23240188 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranosyl trichloroacetimidate | HCID 21631547 | 53% |
Reaction Steps
1.5 ml (15.10-3 mol) of trichloroacetonitrile and 70 mg of NaH (2.3.10-3 mol of NaH in 80% dispersion) are added to a solution of 1 g (3.42.10-3 mol) of 2, 3, 4 -tri-O-acetyl-5-thio-α-D-xylopyranose in 10 ml of methylene chloride. After 4 h at room temperature, the reaction medium is filtered on silica in methylene chloride and then purified by chromatography on silica gel using a hexane/ethyl acetate mixture (3/1 v/v) as the eluent. 790 mg (yield: 53%) of the expected product are obtained after crystallization from an ethyl acetate/hexane mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246961 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-aa359b71c3c249e1a1f6ac726e50d826 |
| Source note | uspto-grants-1993_09 |