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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | alpha-Chloro-o-xylene | HCID 11093 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59186598 | HCID 59186598 | 44.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585858B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-44680852f5a44dc38797a30ef8b5c9cd |
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| Source note | uspto-grants-2009_09 |
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