HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323357Generated: October 25, 2026
Ethyl Acetate → 1-(2-methoxy-5-(1H-tetrazol-1-yl)benzoyl)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine
https://huagongshe.com/reaction/323357
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methoxy-5-(1H-tetrazol-1-yl)benzoyl Chloride | HCID 15392022 | — |
| Reactant | (-)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine (R,R)-di-p-anisoyltartaric acid | HCID 70109704 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | 1-(2-methoxy-5-(1H-tetrazol-1-yl)benzoyl)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine | HCID 18464456 | — |
Reaction Steps
Add (−)-3-phenyl-3-(2-hydroxyethyl)pyrrolidine (R,R)-di-p-anisoyltartaric acid salt (6.72 g, 11.0 mmol) and sodium bicarbonate (4.87 g, 58 mmol) in acetone/water (50 mL/50 mL). Cool in an ice bath. Add a solution of 2-methoxy-5-(1H-tetrazol-1-yl)benzoyl chloride (1.66 g, 9.9 mmol) in acetone (100 mL). After 30 minutes, warm to ambient temperature. After 60 hours, filter the reaction mixture and dilute the filtrate with ethyl acetate. Extract the filtrate with a saturated aqueous sodium bicarbonate solution and then brine. Dry the organic layer over MgSO4, filter, and evaporate in vacuo to give residue. Chromatograph the residue on silica gel eluting sequentially with ethyl acetate, 3% methanol/ethyl acetate, and then 5% methanol/ethyl acetate to give the title compound: Rf=0.48 (5% methanol/dichloromethane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211199B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-7ad8846c5c8e4e0eac0ad3034374efbc |
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| Source note | uspto-grants-2001_04 |
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