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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193833Generated: November 2, 2026

Methyl (2R)-2-oxiranecarboxylate → HCID 56955302, compound

https://huagongshe.com/reaction/2193833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (2R)-2-oxiranecarboxylateHCID 9877347—
ReactantHCID 178419650HCID 178419650—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56955302HCID 56955302—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of Li2CuCl4 (0.2 M in THF, 125 mL, 25.0 mmol) was added slowly to a suspension of cyclopentylmagnesium bromide (2 M in diethyl ether, 135 mL, 270 mmol; Aldrich Chemical Company, Inc., Milwaukee, Wis.) and THF (500 mL) at −50° C. over 2-3 mins. The pale grey/brown suspension was then allowed to warm slowly to −10° C. over 30 mins, by which time the color had developed to a dark grey. The mixture was re-cooled to −78° C. and (R)-methyl oxirane-2-carboxylate (25.0 g, 245 mmol; Aldrich Chemical Company, Inc., Milwaukee, Wis.) was added neat via syringe over 90 seconds. The reaction was then stirred at −78° C. for 20 mins, before removing the ice-bath and allowing to warm to approximately −50° C. over 30 mins. Saturated NH4Cl (aq, 700 mL) was then added and the mixture stirred for 30 mins. The organic layer was collected and the aqueous layer extracted with diethyl ether (2×250 mL). The combined organics were washed with saturated NH4Cl (aq, 350 mL), dried over MgSO4, and evaporated. Distillation of the crude residue (68-70° C. at 0.8 mbar) yielded 65-70% of (I-1b) as a pale yellow oil. A small amount of less volatile material remained in the still pot. 1H NMR (400 MHz; CDCl3): δ 4.17 (1 H), 3.76 (3 H), 2.67 (1 H), 2.01 (1 H), 1.48-1.88 (8 H), 1.11 (2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329920B2
Source datasetuspto-grants-2012_12
ORD IDord-25cc948ef187402888dd93e71c27449d
Source noteuspto-grants-2012_12