HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878781Generated: October 31, 2026
Ammonium Chloride → HCID 68289638, compound
https://huagongshe.com/reaction/878781
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-(Methylthio)-3-pyridinecarboxaldehyde | HCID 45083791 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68289638 | HCID 68289638 | 32% |
Reaction Steps
To a solution of 2-(methylthio)pyridine-5-carbaldehyde (2000 mg, 12.97 mmol) in tetrahydrofuran (20 mL) was added a solution of 0.5 mol/L cyclopropylmagnesium bromide in tetrahydrofuran (28.6 mL) at −40° C. under argon atmosphere. The reaction solution was stirred at the same temperature for 10 minutes, and then slowly warmed to 0° C. and stirred for 1 hour. To the reaction solution was added aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=70:30→60:70) to give cyclopropyl[2-(methylthio)pyrimidin-5-yl]methanol (822 mg, 32%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987445B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-c483cc2b908b4a009037e7fdc5ff34c5 |
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| Source note | uspto-grants-2015_03 |
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