HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859216Generated: November 1, 2026
Tetrahydrofuran → HCID 17608004, compound
https://huagongshe.com/reaction/859216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 68614531 | HCID 68614531 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 17608004 | HCID 17608004 | 85% |
Reaction Steps
A suspension of 7.12 g (20.7 mmol) of (RS)-1-[4-(4-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methyl ester in 10.3 ml of a solution of sodium hydroxide (1N) is prepared and tetrahydrofurane is added until a clear solution is obtained. The mixture is heated to 50° C. for 1 hour. For the working-up, the tetrahydrofurane is evaporated under reduced pressure. The white suspension obtained is diluted with water, then filtered. The white product is treated with toluene and evaporated under reduced pressure to remove most of the water. The azetropic distillation is repeated three times. There are obtained 5.78 g (85% of theory) of (RS)-1-[4-(4-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07151111B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-e2d23dfd230e430ea84bd6ec1f033808 |
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| Source note | uspto-grants-2006_12 |
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