HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13829314, compound → HCID 11608251, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13829314 | HCID 13829314 | — |
| Reactant | HCID 53768393 | HCID 53768393 | — |
| Product | HCID 11608251 | HCID 11608251 | — |
| Product | HCID 12900881 | HCID 12900881 | — |
Reaction Steps
When it is subjected to methanolysis (i.e., heated under reflux in 9% hydrochloric acid-dry methanol), it gives 1 mol each of methylgalactoside, methylarabinoside and methylglucuronide, and 2 mols of methylglucoside. A completely methylated compound (C77H132O29) obtained by methylation of soyasaponin A1 with methyl iodide, dimethyl sulfoxide and sodium hydride gives 1 mol each of methyl 3,4-di-O -methylglucopyranoside, methyl 3,4,6-tri-O -methylgalactopyranoside and methyl 2,4-di-O-methylarabinopyranoside, and 2 mols of methyl 2,3,4,6-tetra-O-methylglucopyranoside when subjected to methanolysis after reduction. It also gives 1 mol of 3,22,24-tri-O-methyl soyasapogenol A (C33H56O4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04524067 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-cf933160d96e4699a6c526daa00f6d97 |
| Source note | uspto-grants-1985_06 |