HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70882Generated: October 27, 2026
Potassium Carbonate → (S)-benzyl 1-(2-tert-butoxy-2-oxoethyl)pyrrolidine-2-carboxylate
https://huagongshe.com/reaction/70882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | Proline benzyl ester hydrochloride | HCID 2733413 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-benzyl 1-(2-tert-butoxy-2-oxoethyl)pyrrolidine-2-carboxylate | HCID 59607548 | 49.4% |
Reaction Steps
To a suspension of (S)-benzyl pyrrolidine-2-carboxylate hydrochloride (700 mg, 2.90 mmol) and K2CO3 (1201 mg, 8.69 mmol) in DMF (7 ml), t-butyl bromoacetate (0.535 ml, 3.62 mmol) is added. After stirring for 71 hours, aqueous K2CO3 (1.5 g of K2CO3/40 ml of H2O) is added to the reaction mixture. The products are extracted with EtOAc. The organic layer is washed twice with water and once with brine, dried over K2CO3, filtered, and concentrated to give (S)-benzyl 1-(2-tert-butoxy-2-oxoethyl)pyrrolidine-2-carboxylate (458 mg); HPLC retention time=1.38 minutes (condition D); MS (m+1)=320.2; 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.44 (s, 9 H) 1.81-2.03 (m, 3 H) 2.13-2.14 (m, 1 H) 2.82-2.88 (m, 1 H) 3.13-3.17 (m, 1 H) 3.46 (A of AB, J=17.3 Hz, 1 H) 3.49 (B of AB, J=17.3 Hz, 1 H) 3.73 (dd, J=8.8 and 4.8 Hz, 1 H) 5.15 (A of AB, J=12.4 Hz, 1 H) 5.17 (B of AB, J=12.4 Hz, 1 H) 7.29-7.38 (m, 5 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822534B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-e5818882a6164ceba0db737e26bdcea1 |
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| Source note | uspto-grants-2014_09 |
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