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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 909975Generated: October 27, 2026

Glycolic Acid → 2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanol

https://huagongshe.com/reaction/909975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycolic AcidHCID 757—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methyl-2-adamantyl chloroacetateHCID 10332006—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanolHCID 5810596767.1%

Reaction Steps

37.6 g (494 mmol) of glycolic acid, 700 mL of DMF, 86.5 g (626 mmol) of potassium carbonate, and 28.3 g (170 mmol) of potassium iodide were added to a 2 L three-neck flask equipped with a thermometer, a cooling pipe, and a stirring apparatus, and then stirred for 30 minutes at room temperature. Subsequently, a solution of 300 mL of dimethylformaldehyde with 100 g (412 mmol) of 2-methyl-2-adamantyl chloroacetate was gradually added thereto. Then, the resultant was heated at 40° C., and stirred for 4 hours. After the reaction, 2,000 mL of diethylether was added thereto and filtrated, thereby obtaining the solution (filtrate). The solution thus obtained was washed three times using 500 mL of distilled water. Thereafter, crystallization was conducted using a mixture solvent of 300 mL of toluene and 200 mL of heptane, thereby obtaining 78 g of the intended compound in the form of a colorless solid (yield: 67%, GC purity: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08021823B2
Source datasetuspto-grants-2011_09
ORD IDord-80a4b0ea87fa4904bb3574ed22b5f4e2
Source noteuspto-grants-2011_09