HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729648Generated: October 26, 2026
Benzyl Bromide → 2-(Benzylthio)pyrimidine-4,6-diol
https://huagongshe.com/reaction/729648
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178516656 | HCID 178516656 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 2-(Benzylthio)pyrimidine-4,6-diol | HCID 178516652 | — |
Reaction Steps
A solution of sodium hydroxide (3.30 g) in ethanol/H2O (60 ml/60 ml) was added to 2-mercaptopyrimidine-4,6-diol (10.00 g) and the mixture stirred for 10 min. Benzyl bromide (13.45 g) was then added dropwise and the mixture heated at 60° C. for 2 h. The reaction was cooled to 0° C. for 1 h before the precipitate was filtered and washed with H2O (100 ml) and then dried in vacuo to afford the subtitle compound as a cream solid. Yield: 15.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582644B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-46f359b68cda47b3b99655e253687da9 |
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| Source note | uspto-grants-2009_09 |
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