HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064787Generated: October 30, 2026
Tetrahydrofuran → Ethyl N-boc-L-proline-4-ene
https://huagongshe.com/reaction/2064787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(1,1-Dimethylethyl) 2-ethyl (2S)-5-oxo-1,2-pyrrolidinedicarboxylate | HCID 5461186 | — |
| Reactant | Lithiumtriethylborohydride | HCID 23664628 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl N-boc-L-proline-4-ene | HCID 10562087 | — |
Reaction Steps
At −50° C. a solution of lithium triethylborohydride in THF (1.0 M, 107 mL, 1.07 eq) is added dropwise to a solution of (S)-5-oxo-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (100 mmol, 1.0 eq) in toluene (170 mL). After 45 min DIPEA (450 mmol, 4.5 eq) and powdered DMAP (1.31 mmol) are added slowly at −50° C. The mixture is treated with trifluoroacetic anhydride (120 mmol, 1.20 eq) while keeping the internal temperature below −45° C., allowed to reach RT within 90 min and stirred for additional 17 h. At 0° C. water (250 mL) is added slowly and the layers are separated. The organic layer is washed with ice-cold water (3×250 mL) and concentrated in vacuo to give the desired product as an orange liquid. LC-MS (acidic): tR=0.93 min; [M+H]+=242.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288435B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-50290cd7c0c1438484fa5db5af72bb42 |
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| Source note | uspto-grants-2012_10 |
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