HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16336Generated: October 29, 2026
Tetrahydrofuran → [(2R,5S)-5-(3,4,5-trifluorophenyl)pyrrolidin-2-yl]methanol
https://huagongshe.com/reaction/16336
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | ethyl (2R,5S)-5-(3,4,5-trifluorophenyl)pyrrolidine-2-carboxylate | HCID 67373176 | — |
| Solvent | Water | HCID 962 | — |
| Product | [(2R,5S)-5-(3,4,5-trifluorophenyl)pyrrolidin-2-yl]methanol | HCID 67463895 | 97.5% |
Reaction Steps
LAH (483 mg) was added to a THF solution (50 mL) of (2R,5S)-5-(3,4,5-trifluorophenyl)pyrrolidine-2-carboxylic acid ethyl ester (2.91 g) over 1 hr at −15° C. The resulting reaction solution was stirred at −15° C. for 19 hr. To the reaction solution, water (0.5 mL), a 5 N sodium hydroxide aqueous solution (0.5 mL), and water (1.5 mL) were added in this order. The resulting mixture was stirred at room temperature for 30 min and then filtered through Celite. The filtrate was concentrated under reduced pressure to give 2.4 g of the title compound. The physical property values of this compound were as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737141B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-06216df421d042e5a78da4bf596942dd |
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| Source note | uspto-grants-2010_06 |
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