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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555202Generated: October 26, 2026

Formaldehyde → 2,2-Adamantane dimethanol

https://huagongshe.com/reaction/555202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantAdamantanoneHCID 64151—
ReactantChloroacetateHCID 518964—
ReactantAdamantane-2-carbaldehydeHCID 12470455—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2,2-Adamantane dimethanolHCID 57874008—

Reaction Steps

To a mixture of 283 g of 2-adamantane carbaldehyde (which had been synthesized by Darzen reaction of adamantanone with chloroacetate, hydrolysis of the resulting glycidyl ester, and subsequent heating for decarbonation), 300 g of tetrahydrofuran, and 500 ml of methanol under ice cooling, 380 g of a 37% formaldehyde aqueous solution was added and then 350 g of a 25% sodium hydroxide aqueous solution was added dropwise over 30 minutes. After the completion of dropwise addition, the ice bath was removed, and the reaction mixture was stirred for 18 hours at room temperature. The reaction mixture was poured into a saturated sodium chloride aqueous solution, which was extracted with a 1:1 tetrahydrofuran/ethyl acetate mixture. The crude product obtained by concentrating the organic layer was recrystallized from n-hexane/diethyl ether, collecting 288 g (yield 85%) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053165B2
Source datasetuspto-grants-2011_11
ORD IDord-f366247e4fda4f1d8b51566fcf81c06a
Source noteuspto-grants-2011_11