HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681873Generated: October 26, 2026
Benzyl Alcohol → Benzyl 1,4,5,6-Tetrahydropyrimidine-5-carboxylate Hydrochloride
https://huagongshe.com/reaction/1681873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1,4,5,6-Tetrahydropyrimidine-5-carboxylic acid hydrochloride | HCID 70342184 | — |
| Product | Benzyl 1,4,5,6-Tetrahydropyrimidine-5-carboxylate Hydrochloride | HCID 20080426 | 76% |
Reaction Steps
1,4,5,6-Tetrahydropyrimidine-5-carboxylic acid hydrochloride (1.0 g, 6.1 mmol) was suspended in dry benzyl alcohol (20 ml). To the mixture was added thionyl chloride (0.76 g, 6.39 mmol) and the resulting mixture was heated in an oil bath at 80° C. for 24 h. The clear solution was poured to anhydrous ethyl ether (100 ml) to induce precipitation. The white solids were collected and crystallized from methanol/THF to give 1.18 g (76%) of product (mp 113°-114° C.). 300 MHz nmr indicated the product. Microanalysis calc.: C 56.58, H 5.89, N 11.00; found: C 56.34, H 6.03, N 11.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05175166 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-a713f6be2aa04ac2bddbc2d06f5e6cef |
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| Source note | uspto-grants-1992_12 |
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