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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111849Generated: October 30, 2026

Methyl iodide → HCID 22765513, compound

https://huagongshe.com/reaction/1111849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
Reactant4,4,6-Trimethylbicyclo[4.2.0]octan-2-oneHCID 22765515—
CatalystMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductHCID 22765513HCID 2276551397%

Reaction Steps

To 0.97 g. (0.04 g. atom) of magnesium in a 250 ml. 3-necked round bottomed flask fitted with dropping funnel, magnetic stirrer, and nitrogen inlet was added 25 ml. of ether. Then 5.0 g. (0.035 mole) of methyl iodide in 100 ml. of ether was added from a dropping funnel at such a rate that reflux was maintained as the Grignard reagent was formed. After all the methyl iodide was added, the solution was stirred and refluxed for an additional 1 hour. Then, 4.98 g. (0.03 mole) of 4,4,6-trimethylbicyclo[4.2.0]octane-2-one was added in 75 ml. of ether over 30 minutes. After all of the ketone was added, the solution was stirred for an additional 1 hour and then 50 ml. of saturated aqueous ammonium chloride was added. The layers were separated and the aqueous layer was extracted twice with 50 ml. portions of ether. The combined ether layers were dried over sodium sulfate and concentrated in vacuo to yield a solid which was sublimed. The recovered product was 5.3 g. (0.029 mole, 97% yield) of 2,4,4,6-tetramethylbicyclo[4.2.0]octane-2-ol. m.p. 54° - 55° C. nmr: (deuterochloroform): 0.92δ (S-34); 1.02δ (S-34); 1.13δ (S-34); 1.21δ (S-34); 1.28δ - 2.25δ (complex multiplets-10H). IR: 3610 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04119575
Source datasetuspto-grants-1978_10
ORD IDord-d5d78c1525394696924ead5e640d3e36
Source noteuspto-grants-1978_10