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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353166Generated: October 30, 2026

tert-Butanol → methyl 2-methyl-6-[(1R,3S)-3-(2-oxoethoxy)cyclohexyloxymethyl]benzoate

https://huagongshe.com/reaction/1353166

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium periodateHCID 23667635—
ReactantHCID 58864607HCID 58864607—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Productmethyl 2-methyl-6-[(1R,3S)-3-(2-oxoethoxy)cyclohexyloxymethyl]benzoateHCID 58864603—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.0 g of methyl 2-((1R,3S)-3-allyloxycyclohexyloxymethyl)-6-methylbenzoate is dissolved in 30 ml of diethyl ether, and 2.0 g of sodium periodate, dissolved in 30 ml of water, are added. At 0° C., 2 ml of a solution of 2.5% by weight of osmium tetroxide and tert-butanol are added. The reaction mixture is stirred vigorously for three hours. The mixture is then cooled to 0° C., and 50 ml of a saturated sodium thiosulfate solution are added. The organic phase is removed. The aqueous phase is extracted three times with in each case 20 ml of diethyl ether. The combined organic phases are dried over magnesium sulfate and the solvent is then removed under reduced pressure. This gives 1.0 g of methyl 2-methyl-6-[(1R,3S)-3-(2-oxoethoxy)cyclohexyloxymethyl]benzoate as a yellow oil C18H24O5 (320.39), MS(ESI): 321 (M+H+), Rf=0 23 (n-heptane:ethyl acetate=1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220876B2
Source datasetuspto-grants-2007_05
ORD IDord-6b8544f26c8940a39d3e21cdba91d550
Source noteuspto-grants-2007_05