HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291344Generated: October 30, 2026
4-(4-Acetoxybenzoyl)benzyl bromide → 2-[4-(4-acetoxybenzoyl) benzylthio]-3-methylthieno[3,2-d]pyrimidin-4(3H)-one
https://huagongshe.com/reaction/1291344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(4-Acetoxybenzoyl)benzyl bromide | HCID 18919207 | — |
| Reactant | Sodium hydroxide--water (1/1/1) | HCID 23719242 | — |
| Reactant | HCID 178481668 | HCID 178481668 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[4-(4-acetoxybenzoyl) benzylthio]-3-methylthieno[3,2-d]pyrimidin-4(3H)-one | HCID 18919236 | 86% |
Reaction Steps
To a solution of 2-mercapto-3-methylthieno[3,2-d]-pyrimidin-4(3H)-one (1.98 g) and 1N-sodium hydroxide/water (10 ml) in ethanol (30 ml) was added 4-(4-acetoxybenzoyl)benzyl bromide (3.95 g) and the mixture was stirred at 60° C. for 1 hour. This reaction mixture was poured in water and the resulting crystals were collected by filtration, rinsed with water, and recrystallized from ethyl acetate to provide the title compound as colorless solid (3.87 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753664 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-b392a2cb266e473c9bb2f4ade1160704 |
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| Source note | uspto-grants-1998_05 |
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