HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655332Generated: October 30, 2026
Sodium Sulfate → {3-[5-(3-Dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanol
https://huagongshe.com/reaction/655332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]benzoate | HCID 59484848 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {3-[5-(3-Dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanol | HCID 59484942 | — |
Reaction Steps
200 ml of a 1 M solution of diisobutylaluminium hydride in THF are added dropwise with stirring to a solution, kept under nitrogen, of 12.6 g (40.0 mmol) of methyl 3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]benzoate in 200 ml of THF. After the mixture has been stirred at room temperature for 1 hour, 10 ml of a saturated aqueous sodium sulfate solution are added dropwise. The resultant precipitate is filtered off with suction and washed with dichloromethane. The filtrate is dried over sodium sulfate and evaporated. The residue is taken up in a mixture of diethyl ether and petroleum ether. The resultant precipitate is filtered off with suction, washed with petroleum ether and dried in vacuo: {3-[5-(3-dimethylaminopropoxy)pyrimidin-2-yl]phenyl}methanol as colourless crystals; m.p. 95-97° C.; ESI 288 (M+H); HPLC: Rt=2.35 min (method B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071593B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-b639ad1f84e14668a8bf5c1e9a671b16 |
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| Source note | uspto-grants-2011_12 |
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