HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Thiobenzonitrile → 4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranoside
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Thiobenzonitrile | HCID 585058 | — |
| Reactant | 2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranosyl trichloroacetimidate | HCID 21631547 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranoside | HCID 14795332 | 23% |
Reaction Steps
A suspension of 192 mg (0.44.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl trichloroacetimidate, 71 mg (0.52.10-3 mol) of 4-mercaptobenzonitrile, 20 mg (0.15.10-3 mol) of zinc chloride and a 400 pm sieve in 2 ml of acetonitrile is stirred for 4 h under an inert atmosphere. The reaction mixture is then filtered on Celite® in ethyl acetate and subsequently washed with a 1N solution of sodium hydroxide, water and finally a saturated solution of sodium chloride, dried over magnesium sulfate and evaporated under reduced pressure. After precipitation in ether, 42 mg (yield: 23%) of the expected product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05101048 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-ab1daa1e73574f0dbddc632424d9d791 |
| Source note | uspto-grants-1992_03 |