HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 2,3,4-Tri-O-acetyl-6-deoxy-6-phthalimido-1-thio-beta-D-galactopyranose
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Potassium Metabisulfite | HCID 28019 | — |
| Reactant | 2-S-(2,3,4-tri-O-acetyl-6-deoxy-6-phthalimido-beta-D-galactopyranosyl)-2-thiopseudourea | HCID 22818495 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,4-Tri-O-acetyl-6-deoxy-6-phthalimido-1-thio-beta-D-galactopyranose | HCID 12805522 | 80.4% |
Reaction Steps
Chloroform (9.0 ml.) is added to a solution of 2-S-(2,3,4-tri-O-acetyl-6-deoxy-6-phthalimido-β-D-galactopyranosyl)-2-thiopseudourea (3.4 g.) in water (10 ml.) containing potassium metabisulfite (1.38 g.). The mixture is heated with stirring under reflux for 15 minutes. The cooled solution is separated, and the organic layer is dried and evaporated in vacuo to give the title compound (2.5 g.). This material is used directly for the preparation of 6-(5-cholesten-3β-yloxy)hexyl 2,3,4-tri-O-acetyl-6-deoxy-6-ththalimido-1-thio-β-D-galactopyranoside
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310505 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-3e1c7af0f3954cafb88e31b24631eea3 |
| Source note | uspto-grants-1982_01 |