HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548639Generated: October 28, 2026
Hydrochloric Acid → HCID 16662660, compound
https://huagongshe.com/reaction/548639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 57550261 | HCID 57550261 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 16662660 | HCID 16662660 | 88% |
Reaction Steps
Lithium borohydride (0.1 g, 4.92 mmol, 1.8 eq) is added to a solution of methyl 1-{4-[3-(2-methylpyrrolidin-1-yl)propoxy]phenyl}-5-oxopyrrolidine-3-carboxylate a54 (0.99 g, 2.73 mmol, 1 eq) in tetrahydrofuran (20 ml) and methanol (0.35 ml). The mixture is stirred at 75° C. for 1 h, then cooled to 0° C. and a solution of 1 M hydrochloric acid is added. A solution of 2M sodium hydroxide is then added to reach a pH of 10. The aqueous layer is extracted twice with ethyl acetate, then the organic layers are dried over magnesium sulfate, and concentrated under vacuum to give 0.79 g of 4-(hydroxymethyl)-1-{4-[3-(2-methylpyrrolidin-1-yl)propoxy]phenyl}pyrrolidin-2-one 72 as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943605B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-8c45f7c701654165801f42b4caa5b549 |
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| Source note | uspto-grants-2011_05 |
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