HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364992Generated: October 29, 2026
Hydrochloric Acid → (R)-3-[(S)-(3,5-dichlorophenoxy)phenylmethyl]pyrrolidine-1-carboxylic acid t-butyl ester
https://huagongshe.com/reaction/1364992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,3-Dichloro-5-fluorobenzene | HCID 137002 | — |
| Reactant | (r)-3-((s)-Hydroxyphenylmethyl)pyrrolidine-1-carboxylic acid t-butyl ester | HCID 58507559 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-3-[(S)-(3,5-dichlorophenoxy)phenylmethyl]pyrrolidine-1-carboxylic acid t-butyl ester | HCID 66924546 | — |
Reaction Steps
(R)-3-((S)-hydroxyphenylmethyl)pyrrolidine-1-carboxylic acid t-butyl ester (10.0 g, 36.0 mmol) was dissolved in anhydrous DMF (65 mL, 840 mmol). Washed and dried sodium hydride (1.0 g, 43 mmol) was added, and the mixture stirred at room temperature for 15 minutes. 3,5-Dichlorofluorobenzene (10 mL, 80 mmol) was then added, and the mixture stirred at 70° C. for 3 hours. The mixture was cooled to room temperature. EtOAc (200 mL) and 1M HCl (200 mL) was added, mixed, and the phases separated. The organic layer was washed with 2×200 mL of diluted aqueous NaCl, dried over Na2SO4, and concentrated to dryness to yield 19 g of crude product. The crude product was purified on a 300 g SiG column to yield (R)-3-[(S)-(3,5-dichlorophenoxy)phenylmethyl]pyrrolidine-1-carboxylic acid t-butyl ester as a white sticky foam (14.1 g, 91.67% purity).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888386B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-62d57ef0686f4a399195fe4ce4c288ff |
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| Source note | uspto-grants-2011_02 |
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