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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610467Generated: October 30, 2026

Methyl iodide → HCID 12425357, compound

https://huagongshe.com/reaction/610467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantBenzyl acetoacetateHCID 142266—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12425357HCID 12425357—

Reaction Steps

Following the procedure of Weiler, J. Am. Chem. Soc. 1974, 96, 1082, benzyl acetoacetate, 7.68 g (40 mmol) was added dropwise to a 0° C. suspension of sodium hydride (2.1 g of 50% dispersion, 42 mmol) in THF (100 mL). After stirring for 10 minutes n-butyl lithium (16 mL of 2.5 M in hexane) was added and the mixture was aged for an additional 10 minutes. At this time iodomethane (2.74 mL, 44 mmol) in THF (4 mL) was added dropwise and the mixture aged 1 hour while slowly warming to room temperature. Work-up was achieved by quenching at 0° C. with 1N HCl, extracting with ether, washing the ether with aqueous NaHCO3, brine, and drying with MgSO4. Removal of the solvent yielded benzyl 3-oxopentanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998612
Source datasetuspto-grants-1999_12
ORD IDord-db6f33b4d57d44f385a24e130604ee9b
Source noteuspto-grants-1999_12