HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253552Generated: October 26, 2026
Ammonium Chloride → Tert-butyl 3-(1-hydroxy-5-methoxy-1-phenylpentyl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/253552
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 3-benzoylpyrrolidine-1-carboxylate | HCID 57419606 | — |
| Reactant | HCID 178495008 | HCID 178495008 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 3-(1-hydroxy-5-methoxy-1-phenylpentyl)pyrrolidine-1-carboxylate | HCID 57786486 | 44% |
Reaction Steps
A stirred solution of tert-butyl 3-benzoylpyrrolidine-1-carboxylate (489 mg, 1.78 mmol) in dry THF (10 mL) was cooled to −70° C. and 2 M 4-methoxybutylmagnesium chloride in THF (8 mL, 16 mmol) was added. The mixture was stirred at −70° C. for 1 h and poured into satd aq NH4Cl (100 mL). The mixture was extracted with ether (2×100 mL) and the combined ether extracts were dried over Na2SO4. Removal of the solvent left an oil which was purified by flash chromatography on a 40-g silica cartridge eluted with a 0 to 100% ethyl acetate in hexanes gradient to afford tert-butyl 3-(1-hydroxy-5-methoxy-1-phenylpentyl)pyrrolidine-1-carboxylate (290 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07872028B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-4012d03427a04d28a4a247d17b6de104 |
|---|
| Source note | uspto-grants-2011_01 |
|---|