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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103004Generated: November 1, 2026

Methyl formate → HCID 86605476, compound

https://huagongshe.com/reaction/2103004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
ReactantSodium hydrideHCID 24758—
ReactantHCID 69054496HCID 69054496—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86605476HCID 86605476—

Reaction Steps

To a solution of 6-(methoxymethoxy)--5,7,8-trimethylspiro[chromene-2,1′-cyclobutan]-4(3H)-one (2.0 g) in 20 mL of THF was added under stirring, NaH (1.38 g). After 5 minutes, 8.5 mL of methyl formate (137.4 mmol) were added dropwise to the mixture. The reaction was allowed to stir at room temperature overnight. The organic phase was washed with 1N HCl and water, dried over anhydrous MgSO4, and concentrated in vacuo to give 6-(methoxymethoxy)-5,7,8-trimethyl-4-oxo-3,4-dihydrospiro[chromene-2,1′-cyclobutane]-3-carbaldehyde as a yellow paste. This intermediate was used directly for subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576094B2
Source datasetuspto-grants-2009_08
ORD IDord-b18583ccf8314f64a96d78d0f28b036e
Source noteuspto-grants-2009_08