HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461012Generated: October 26, 2026
Triethylamine → 7-Hexanoyloxymethyl theophylline
https://huagongshe.com/reaction/461012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-Hydroxymethyl theophylline | HCID 64134 | — |
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | Dichloromethane heptane | HCID 21907733 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Hexanoyloxymethyl theophylline | HCID 23455170 | 43.7% |
Reaction Steps
To 0.71 g (0.0053 mole) of hexanoyl chloride in 10 ml of CH2Cl2 there was added 1.10 g (0.0052 mole) of 7-hydroxymethyl theophylline; no reaction occurred and the reaction mixture was a suspension. Then 0.58 g (0.0057 mole) of triethylamine was added and a clear, colorless solution was obtained. The solution was stirred at room temperature for 15 minutes then concentrated in vacuo. The residue was titrated with 200 ml ether and filtered. The filtrate was concentrated in vacuo to give an oil which was titrated with heptane CH2Cl2 (50:10). The resulting suspension was filtered while hot and concentrated to 20 ml, then cooled to room temperature. A gelatinous mass precipitated which was filtered and dried to give 0.70 g (mp 67°-72° C, 43% yield) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061753 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-fafaa4ce559646a580a7394a4a269550 |
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| Source note | uspto-grants-1977_12 |
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