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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603872Generated: October 30, 2026

Phosphorus oxychloride → 2-(Benzyloxymethyl)-6-chromanecarbaldehyde

https://huagongshe.com/reaction/1603872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium AcetateHCID 517045—
Reactant2-(Benzyloxymethyl)chromaneHCID 19606315—
SolventDichloromethaneHCID 6344—
Product2-(Benzyloxymethyl)-6-chromanecarbaldehydeHCID 1960632853%

Reaction Steps

Phosphorous oxychloride (0.863 ml, 9.26 mmol) was added very slowly and under inert atmosphere on N-methylformanilide (1.14 ml, 9.26 mmol) and the mixture was left under stirring at room temperature for 30 minutes. After that 2-(benzyloxymethyl)chromane (1.569 g, 6.18 mmol) was added stirring at 65° C. for 1.5 h. Subsequently the mixture was diluted with dichloromethane (30 ml), added with a 15% sodium acetate solution (20 ml), the phases were separated and the organic phase was washed successively with a 1M hydrochloric acid solution and a sodium chloride saturated solution. After drying and removing the solvent by evaporation under reduced pressure, a residue was obtained which was purified by flash chromatography through a silica gel column. Eluting with hexane:ethyl acetate, 10:1, 0.921 g of the title product were recovered (53% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990142
Source datasetuspto-grants-1999_11
ORD IDord-97ffed544321446daab1e02edea57de1
Source noteuspto-grants-1999_11