HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 13325399, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromoheptane | HCID 12369 | — |
| Reactant | HCID 13325464 | HCID 13325464 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13325399 | HCID 13325399 | 65.3% |
Reaction Steps
To 20 ml. of a 50% aqueous acetone solution were added 2.92 g. of 2,3,4-tri-O-acetyl-1-thio-β-D-xylopyranoside (17) and 1.79 g. of n-heptyl bromide. To the solution was further added 1.38 g. of potassium carbonate and then a boiling under reflux was carried out for one hour. After completion of the reaction, the solution was neutralized with acetic acid, extracted with chloroform washed with water, and dried. The used solvent was distilled away to obtain 2.55 g. of colorless oily n-heptyl 2,3,4-tri-O-acetyl-1-thio-β-D-xylopyranoside (18). The yield was 65.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04454123 |
| Source dataset | uspto-grants-1984_06 |
| ORD ID | ord-9728c824601d4859bcd0438fff4bcfdf |
| Source note | uspto-grants-1984_06 |