HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614944Generated: October 30, 2026
Triethylamine → 9-(3-Benzoyloxypropoxymethyl)guanine
https://huagongshe.com/reaction/614944
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 14655183 | HCID 14655183 | — |
| Reactant | Guanine | HCID 135398634 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 9-(3-Benzoyloxypropoxymethyl)guanine | HCID 135968531 | 21.2% |
Reaction Steps
A solution of trimethylsilylated guanine in benzene (25 ml) prepared as in Example 6 (from 2.0 g of guanine) containing triethylamine was heated at reflux and 3-benzoyloxypropoxymethyl chloride (2.96 g) dissolved in benzene (15 ml) was added over a 3 hour period. The reaction mixture was heated at reflux under nitrogen overnight. The solvent was removed under reduced pressure, and 95% ethanol and methanol were added to the residual oil. The mixture was heated on a steam bath for several minutes and the solvent then evaporated under reduced pressure. Chloroform (200 ml) was added and the resulting solid removed by filtration. The solid was dissolved in a minimal amount of DMF, filtered (to remove any guanine present) and reprecipitated by the addition of water. Recrystallization from methanol (with charcoaling) gave 9-(3-benzoyloxypropoxymethyl)guanine (0.94 g) as a pale yellow solid, m.p. 198°-201° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04146715 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-30af602cad0043feb25628c8646941f6 |
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| Source note | uspto-grants-1979_03 |
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