HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260305Generated: October 26, 2026
Sodium ethoxide → 5-Bromo-2-(propan-2-yl)pyrimidine-4-carboxylic acid
https://huagongshe.com/reaction/1260305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-Methylpropanimidamide hydrochloride | HCID 2782053 | — |
| Reactant | Mucobromic Acid | HCID 3033972 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-2-(propan-2-yl)pyrimidine-4-carboxylic acid | HCID 67299898 | 73% |
Reaction Steps
To a stirred suspension of isobutyramidine hydrochloride (6.47 g, 47.5 mmol) at r.t. in EtOH (30 ml) under an argon atmosphere was added sodium ethylate solution (21 ml, 21% in EtOH) over 5 min. The suspension was heated to 50° C. and a solution of mucobromic acid (5.7 g, 22.1 mmol) in EtOH (24 ml) was added dropwise over 5 min at 50° C. An additional portion of sodium ethylate solution (12 ml, 21% in EtOH) was added dropwise over 5 min. The mixture was then cooled to r.t. The solids were filtered off, and the cake was washed with plenty of ethanol. The filtrate was concentrated to leave the crude product as a light brown solid. The crude material was triturated in 2 N HCl (100 ml). The product was collected by filtration, washed with plenty of H2O and plenty of n-heptane and dried to give the product (2.09 g, 73%) as beige solid. MS: M=244.9 (M−H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470820B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-0b607528516c456abb1bf9a6dead1d05 |
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| Source note | uspto-grants-2013_06 |
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