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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908944Generated: November 1, 2026

Sulfuric Acid → HCID 67997342, compound

https://huagongshe.com/reaction/1908944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant1,1-DichloroethaneHCID 6365—
ReactantMethacryloyl chlorideHCID 13528—
ReactantHCID 67997339HCID 67997339—
SolventPyridineHCID 1049—
ProductHCID 67997342HCID 6799734240.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

In a flask equipped with a stirrer, a thermometer, a dropping funnel, and a Dimroth condenser, 50 g of 3-(1-hydroxy-1-methylethyl)adamantane-1-carboxylic acid t-butyl ester, 200 mL of dichloroethane, and 80 g of pyridine were put, and 71.7 g of methacrylic acid chloride was dropped thereto at 60° C. over 2 hours. After the dropping was completed, the resultant substance was stirred at 60° C. for another 8 hours. Then, the resultant substance was neutralized with 320 g of 10% aqueous solution of sulfuric acid while the flask was ice-cooled. The reaction solution was separated into an organic layer and a water layer. The organic layer was washed twice with 500 mL of ion exchanged water, and then was concentrated. The obtained raw product was purified by silica gel column chromatography. As a result, 25 g of 3-(1-methacryloyloxy-1-methylethyl)adamantane-1-carboxylic acid t-butyl ester was obtained as a white solid. White solid 2, which was obtained, was identified with 1H-NMR, 13C-NMR and IR (see FIGS. 2, 3 and 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598292B2
Source datasetuspto-grants-2013_12
ORD IDord-f4fac172d69c4b7187caecbfa17347c0
Source noteuspto-grants-2013_12