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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859762Generated: November 1, 2026

Formaldehyde → HCID 18626562, compound

https://huagongshe.com/reaction/1859762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactantethyl 9H-xanthene-9-carboxylateHCID 235688—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 18626562HCID 1862656268%

Reaction Conditions

Temperature-50 °C

Reaction Steps

A mixture of 1.5 g (5.9 mmol) of ethyl 9H-xanthene-9-carboxylate in 20 ml of THF and 1.6 ml of DMPU under an inert atmosphere is cooled to −50° C. 4 ml (6.4 mmol) of BuLi (1.6 M in hexane) are added dropwise to this medium with stirring, and the medium is then left stirring for 10 minutes at −40° C. After allowing the reaction medium to warm to 10° C., a flow of formaldehyde generated from 5.4 g (0.18 mol) of sublimed paraformaldehyde entrained by a stream of nitrogen is bubbled in. After stirring for 2 hours at room temperature, the suspension is dispersed in 50 ml of water. The reaction medium is then extracted twice with 100 ml of ether. The combined organic phases are dried over Na2SO4. After evaporation, the residual oil is chromatographed on silica. Eluent: CH2Cl2. 1.1 g of a yellow oil are obtained (yield: 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528538B1
Source datasetuspto-grants-2003_03
ORD IDord-efa3bfceeb1b4119ab06b2156f3e3855
Source noteuspto-grants-2003_03