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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564219Generated: October 25, 2026

Ammonium Hydroxide → (R)-tert-butyl 2-(5-methoxycarbonylthiophen-2-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/564219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantMethyl 5-bromothiophene-2-carboxylateHCID 605713—
ReactantN-Boc-pyrrolidineHCID 643455—
ReactantSparteineHCID 644020—
ReactantTri-t-butylphosphine fluoroborateHCID 44558591—
ReactantCID 53628100HCID 178418400—
Catalystpalladium(II) acetateHCID 167845—
CatalystZincchlorideHCID 3007855—
SolventDiethyl EtherHCID 3283—
SolventCyclohexaneHCID 8078—
Solventtert-Butyl methyl etherHCID 15413—
Product(R)-tert-butyl 2-(5-methoxycarbonylthiophen-2-yl)pyrrolidine-1-carboxylateHCID 66758892—

Reaction Steps

To a solution of N-Boc-pyrrolidine (3 mL) and (−)-sparteine (3.9 mL) in tert-butyl methyl ether (36 mL) at −78° C. was added 1.4M sec-butyl lithium in cyclohexane (12.21 mL). The solution was stirred for 3 hours and 1M zinc chloride in ether (10.2 mL) was added. The mixture was stirred for 30 minutes and warmed to ambient temperature for 30 minutes. Methyl 5-bromothiophene-2-carboxylate (3.15 g), tri-tert-butylphosphine tetrafluoroborate (249 mg) and palladium(II) acetate (153 mg) were added, and the mixture was stirred at ambient temperature overnight, treated with concentrated ammonium hydroxide (1 mL) and stirred for 30 minutes, and filtered through diatomaceous earth (Celite®). The filtrate was washed with 0.5M hydrochloric acid solution and water and concentrated. The concentrate was flash chromatographed on silica gel with ethyl acetate/hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067613B2
Source datasetuspto-grants-2011_11
ORD IDord-6c310ccc24894e758f571d8f23d9781f
Source noteuspto-grants-2011_11