HuagongsheHuagongshe Chemistry Print Report · For research reference only
Theophylline → HCID 13041076, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Theophylline | HCID 2153 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Chloromethyl pivalate | HCID 87885 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13041076 | HCID 13041076 | 25.5% |
Reaction Steps
A suspension of 3.60 g (0.02 mole) of theophylline and 1.38 g (0.01 mole) of K2CO3 in 75 ml of acetone was refluxed overnight and then allowed to react at reflux with 3.00 g (0.02 mole) of pivaloxymethyl chloride for 2 days. The suspension was filtered and the residue was washed with acetone (200 ml). The combined filtrate and wash was concentrated in vacuo and the residue was extracted with boiling heptane (200 ml). The heptane solution was cooled in the refrigerator for 0.5 hr then filtered. The residue was dried in vacuo to give 1.50 g (mp 108°-109.5°) of 7-pivaloxymethyl theophylline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061753 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-a312318ca37444f087cf993391e06144 |
| Source note | uspto-grants-1977_12 |