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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062460Generated: November 3, 2026

Ethoxalyl chloride → Ethyl 2-oxoheptanoate

https://huagongshe.com/reaction/1062460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
ReactantLithium iodideHCID 66321—
ReactantHCID 178445865HCID 178445865—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-oxoheptanoateHCID 1174509123.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a suspension of LiI (23.61 g, 176.44 mmol) in THF (200 mL) at rt was slowly added Cu2Br2 (25.30 g, 88.22 mmol). A vigorous exothermic reaction occurred, and the mixture was then cooled to −78° C. Pentylmagnesium bromide (2M, 36.76 mL, 88.22 mmol) was slowly added at −78° C., and followed soon after by ethyl chloro(oxo)acetate (10 g, 73.52 mmol). The resulting solution was stirred 10 minutes at −78° C., then quenched by dropwise addition of water. The mixture was allowed to warm to rt, and then the organic phase was separated, dried (MgSO4), and evaporated. Purification by flash chromatography using 9:1 hexane/EtOAc as eluant gave ethyl 2-oxoheptanoate as a colorless oil (3.0 g, 23%). 1NMR (400 MHz, CDCl3) δ 4.33-4.21 (m, 2 H), 2.82 (m, 2 H), 1.63-1.59 (m, 2 H), 1.63-11.19 (m, p H), 0.9-0.83 (m, 3 H), LC-MS m/z 279.21 (MH+), retention time 2.42 min (method 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960601B2
Source datasetuspto-grants-2005_11
ORD IDord-312c002125714cd29c73ef6c1858903c
Source noteuspto-grants-2005_11