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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284559Generated: October 31, 2026

Aniline → HCID 13564469, compound

https://huagongshe.com/reaction/1284559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantHCID 13560308HCID 13560308—
SolventMethanolHCID 887—
ProductHCID 13564469HCID 1356446949%

Reaction Steps

A mixture of 6-hydroxy-3,4-dihydrobenzopyran-7-carboxaldehyde (429 mg, 2.41 mmol) and aniline (224 mg, 2.42 mmol) in methanol (30 mL) was warmed and the methanol, which distilled over, was collected. When 10 mL of methanol had been collected, the mixture was allowed to cool and the intermediate Schiff's base crystallized out. This material was collected and redissolved in fresh methanol (30 mL). Sodium borohydride (1 molar equiv.) was added in portions and the color immediately discharged. The mixture was concentrated to 50% of its original volume, then poured into an excess of water (100 mL). The aqueous solution was rendered acidic with 2N HCl, filtered to remove any insoluble material, then basified with 7%, NaHCO3. The product, which precipitated, was collected by filtration and dried to afford 6-hydroxy-7-phenylaminomethyl-3,4-dihydrobenzopyran (277 mg, 49%), m.p. 135°-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563476
Source datasetuspto-grants-1986_01
ORD IDord-e4122300dd304b1593bedf98eb030ac4
Source noteuspto-grants-1986_01