HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603872Generated: October 30, 2026
Phosphorus oxychloride → 2-(Benzyloxymethyl)-6-chromanecarbaldehyde
https://huagongshe.com/reaction/1603872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(Benzyloxymethyl)chromane | HCID 19606315 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Benzyloxymethyl)-6-chromanecarbaldehyde | HCID 19606328 | 53% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05990142 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-97ffed544321446daab1e02edea57de1 |
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| Source note | uspto-grants-1999_11 |
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