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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutanolHCID 6560—
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(R)-tert-butyl 2-((R)-(4-hydroxyphenyl)((S)-2-phenylpropanamido)methyl)pyrrolidine-1-carboxylateHCID 67438445—
SolventTetrahydrofuranHCID 8028—
Product(R)-tert-Butyl 2-((R)-(4-isobutoxyphenyl)((S)-2-phenylpropanamido)methyl)pyrrolidine-1-carboxylateHCID 86658403—

Reaction Conditions

Temperature140 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304577B2
Source datasetuspto-grants-2012_11
ORD IDord-37af9dffaaf34b25a7b8166bebf42127
Source noteuspto-grants-2012_11