HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586203Generated: October 29, 2026
Hydrochloric Acid → HCID 54300677, compound
https://huagongshe.com/reaction/586203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (R)-1-(4-chloro-pyrimidin-2-yl)ethyl butyrate | HCID 10944226 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54300677 | HCID 54300677 | 71% |
Reaction Steps
To a solution of (R)-1-(4-chloro-pyrimidin-2-yl)-ethyl butyrate (prepared according to the method of Preparation Seven, 250 mg, 1.1 mmol) in, dioxane (0.9 mL) was added concentrated hydrochloric acid (0.9 mL). This mixture was allowed to stir at room temperature for 5 h, quenched with saturated aqueous sodium bicarbonate followed by solid sodium bicarbonate until no more gas evolution was evident. Dichloromethane was added and the layers were separated. The aqueous phase was extracted with dichloromethane (3×) and the combined organic extracts were dried over sodium sulfate, filtered, and evaporated to give 125 mg (71%) of the title compound as a pale yellow oil. 1H NMR (CDCl3, 400 MHz) δ 8.59 (d, 1H), 7.25 (d, 1H), 4.92 (q, 1H), 3.81 (br s, 1H), 1.56 (d, 3H); MS (APCI) 159, 161 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936600B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-e926a3ded1e84a2d85adabc1348cf57c |
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| Source note | uspto-grants-2005_08 |
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