HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6158Generated: October 26, 2026
Sodium borohydride → 4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propylthio)pyridine
https://huagongshe.com/reaction/6158
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1H-Isoindole-1,3(2H)-dione, 2-[3-(4-pyridinylthio)propyl]- | HCID 19079118 | — |
| Reactant | Ethanol ethylacetate | HCID 21584252 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propylthio)pyridine | HCID 57122505 | 54.4% |
Reaction Steps
To a solution of 5.97 g (20.0 mmol) of 4-(3-phthalimidopropylthio)pyridine in 300 ml of ethanol, 1.51 g (40 mmol) of sodium borohydride was added, and the mixture was stirred at room temperature for 5 hours. The solvent was distilled off and saturated saline was added to the residue. The mixture was extracted with chloroform and the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethanol/ethyl acetate =1:10 to give 3.27 g of the desired compound (54.4% yield, colorless crystals), mp. 132°-134° C. NMR (200 MHz, CDCl3) δ: 2.11 (2H, m), 2.97 (2H, m), 3.72 (2H, m), 5.83 (1H, s), 6.98 (2H, d, J=5.4 Hz), 7.47-7.67 (3H, m), 7.77 (1H, dd, J=7.6, 1.2 Hz), 8.02 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246948 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-f61c39e9b64e46f3aa67a30fba7b886d |
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| Source note | uspto-grants-1993_09 |
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