HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715725Generated: October 30, 2026
Benzyltrimethylammonium hydroxide → (R)-4-Acetyl-1-((S)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-one
https://huagongshe.com/reaction/715725
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | 4-Acetyl-1-[(1S)-1-(4-methoxyphenyl)ethyl]pyrrolidin-2-one | HCID 58072016 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | (R)-4-Acetyl-1-((S)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-one | HCID 58071853 | — |
Reaction Steps
103 g of a mixture of diastereoisomers (R/S)-4-acetyl-1-[(S)-1-(4-methoxyphenyl)-ethyl]-pyrrolidine-2-one is dissolved in 155 mL 1-butanol at 25° C. 18 mL benzyltrimethylammonium hydroxide (40% solution in methanol) is added. The solution is stirred for 30 minutes at 25° C. The solution is cooled to 0° C. Precipitation starts. The suspension is stirred for 15 minutes at 0° C. 100 mL n-heptane is added slowly and the suspension is stirred for 30 minutes at 0° C. The addition of 100 mL portions of n-heptane is repeated 4 times with subsequent stirring of the suspension at 0° C. for 30 minutes. The precipitate is isolated, washed with n-heptane and dried at 50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187478B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-ef2e10cc9990444da5ac7da4fd00888d |
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| Source note | uspto-grants-2015_11 |
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