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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731547Generated: October 29, 2026

alpha-Chloro-o-xylene → HCID 59186598, compound

https://huagongshe.com/reaction/731547

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Chloro-o-xyleneHCID 11093—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59186598HCID 5918659844.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-methylbenzyl chloride (0.579 g, 4.12 mmol) in THF (20 mL) was treated with Mg (0.180 g, 7.50 mmol) and strirred at room temperature until all the Mg had dissolved. The mixture was cooled to 0° C., treated with a solution of 1,4-cyclohexanedione mono-ethylene ketal (0.579 g, 4.12 mmol) in THF (50 mL), warmed to room temperature, stirred overnight, quenched with saturated NH4Cl (100 mL), and extracted with ethyl acetate (3×100 mL). The combined extracts were washed with water and brine, dried (Na2SO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 6:1 hexanes/ethyl acetate to provide the desired product (0.48 g, 44%) MS (ESI) m/e 262 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585858B2
Source datasetuspto-grants-2009_09
ORD IDord-44680852f5a44dc38797a30ef8b5c9cd
Source noteuspto-grants-2009_09