HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070Generated: October 26, 2026
Isopropanol → trans-1-Benzyl-3-hydroxymethyl-4-(2-methoxyphenyl)pyrrolidine
https://huagongshe.com/reaction/1070
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl [trans-1-benzyl-4-(2-methoxyphenyl)pyrrolidin-3-yl]carboxylate | HCID 67661645 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | trans-1-Benzyl-3-hydroxymethyl-4-(2-methoxyphenyl)pyrrolidine | HCID 70344956 | — |
Reaction Steps
To 560 mmol of lithium aluminum hydride in 800 ml of tetrahydrofuran (THF), under a nitrogen atmosphere and at 5° C., are added 225 mmol of methyl [trans-1-benzyl-4-(2-methoxyphenyl)pyrrolidin-3-yl]carboxylate (described in Preparation A) dissolved in 500 ml of THF. After stirring for 1 hour at 5° C., 139 ml of isopropyl alcohol are added slowly to the above mixture, followed by 85.2 ml of saturated sodium chloride solution. The mixture is stirred slowly at room temperature. After filtration and evaporation of the solvents, the expected product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723484 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-aad0c6cdb96e435783b60b50f263f74c |
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| Source note | uspto-grants-1998_03 |
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