HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874650Generated: November 1, 2026
Isobutanol → (R)-tert-Butyl 2-((R)-(4-isobutoxyphenyl)((S)-2-phenylpropanamido)methyl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1874650
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutanol | HCID 6560 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | (R)-tert-butyl 2-((R)-(4-hydroxyphenyl)((S)-2-phenylpropanamido)methyl)pyrrolidine-1-carboxylate | HCID 67438445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-tert-Butyl 2-((R)-(4-isobutoxyphenyl)((S)-2-phenylpropanamido)methyl)pyrrolidine-1-carboxylate | HCID 86658403 | — |
Reaction Steps
A solution of 2-methyl-1-propanol (6.52 μL, 0.071 mmol), DEAD (11.19 μL, 0.071 mmol), and triphenylphosphine (18.53 mg, 0.071 mmol) in THF (520 μL) in a microwave vial was stirred at room temperature for 10 min. (R)-tert-Butyl 2-((R)-(4-hydroxyphenyl)((S)-2-phenylpropanamido)methyl)pyrrolidine-1-carboxylate (30 mg, 0.071 mmol) was added and the solution heated at 140° C. in a microwave (Biotage) for 20 min. The crude mixture was filtered through a plug of silica gel eluting with 50% EtOAc in hexanes. The filtrate was concentrated in vacuo and carried directly into the next reaction. LRMS (ESI) m/e 481.50 [(M+H)+, calcd for C29H41N2O4 481.31].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304577B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-37af9dffaaf34b25a7b8166bebf42127 |
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| Source note | uspto-grants-2012_11 |
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