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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245032Generated: October 27, 2026

Diethyl Ether → HCID 57457956, compound

https://huagongshe.com/reaction/1245032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Benzyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylateHCID 11594288—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
ProductHCID 57457956HCID 5745795672%

Reaction Conditions

Temperature5 °C

Reaction Steps

4.80 g (13.4 mmol) of methyltriphenylphosphonium bromide were added to a suspension of 1.41 g (12.6 mmol) of potassium t-butoxide in 100 ml of diethyl ether, and the resulting mixture was stirred for 15 minutes at 5° C. At the end of this time, a solution of 2.50 g (9.0 mmol) of (S)-1-benzyloxycarbonyl-4-oxoproline methyl ester in 30 ml of diethyl ether was added to the mixture thus obtained, and the mixture was stirred for an additional 3 hours at 35° C. At the end of this time, 50 ml of a saturated aqueous solution of ammonium chloride were added to the reaction mixture with ice-cooling, and the resulting mixture was partitioned. The organic extract thus obtained was washed with water, dried over anhydrous magnesium sulfate and then concentrated by evaporation under reduced pressure. The residue was purified by chromatography on a silica gel column using a 1:3 by volume mixture of ethyl acetate and hexane as the eluant to afford 1.80 g (yield: 72%) of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122666B2
Source datasetuspto-grants-2006_10
ORD IDord-68f09888b6cc4b64af1cecc8360eb43f
Source noteuspto-grants-2006_10