HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440248Generated: October 25, 2026
Methyl iodide → 1-t-Butoxycarbonyl-3-methoxy-4-phenylaminopyrrolidine
https://huagongshe.com/reaction/440248
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-t-Butoxycarbonyl-3-hydroxy-4-phenylaminopyrrolidine | HCID 21473347 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-t-Butoxycarbonyl-3-methoxy-4-phenylaminopyrrolidine | HCID 21473342 | 79.7% |
Reaction Steps
To 10 ml of anhydrous tetrahydrofuran was added 0.34 g (0.0085 mole) of a 60% sodium hydride-mineral oil, and while stirring the mixture at 45° to 50° C., 1.21 g (0.0085 mole) of methyl iodide was added thereto. To the mixture was added dropwise a solution of 2.37 g of 1-t-butoxycarbonyl-3-hydroxy-4-phenylaminopyrrolidine obtained in Reference example 17 (1) dissolved in 10 ml of anhydrous tetrahydrofuran, and the mixture was further stirred at the same temperature for 1 hour. After the mixture was cooled to room temperature, the solvent was removed under reduced pressure, and the residue was supplied to silica gel column chromatography (the eluent used was a mixture of methyl acetate: toluene = 1 : 4) to obtain 1.98 g of 1-t-butoxycarbonyl-3-methoxy-4-phenylaminopyrrolidine as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05519016 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-96053ac08ae847158f1522d21ca752eb |
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| Source note | uspto-grants-1996_05 |
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