HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663573Generated: October 29, 2026
Phenol → (2S)-2-[2-oxo-4-(phenoxymethyl)-1-pyrrolidinyl]butanamide
https://huagongshe.com/reaction/1663573
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenol | HCID 996 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (2S)-2-[4-(hydroxymethyl)2-oxo-1-pyrrolidinyl]butanamide | HCID 60105803 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S)-2-[2-oxo-4-(phenoxymethyl)-1-pyrrolidinyl]butanamide | HCID 60105796 | — |
Reaction Steps
In a 50 ml three necked flask fitted with magnetic stirrer and dropping funnel under inert atmosphere, 1 g (5 mmoles, 1 eq) of (2S)-2-[4-(hydroxymethyl)-2-oxo-1-pyrrolidinyl]butanamide 6 is dissolved in 20 ml of THF and cooled down to 0° C. 517 mg of phenol, 0.87 ml (960 mg) of diethyl azodicarboxylate and 1.44 g of triphenylphosphine (5.5 mmoles, 1.1 eq each) are successively added and the mixture stirred for 2 hours. The mixture is concentrated to dryness and purified by Prep LC (500 kg SiO2, CH2Cl2/EtOH, 97.5:2.5) to give 1.1 g of pure 18, 80%, crystallised from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034958B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-f0809eb32c10470aaa9edc3615552d06 |
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| Source note | uspto-grants-2011_10 |
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