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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115176Generated: October 29, 2026

Hydrochloric Acid → 4-(Dibenzylamino)-6-methoxy-1-naphthaldehyde

https://huagongshe.com/reaction/2115176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantN,N-dibenzyl-7-methoxynaphthalen-1-amineHCID 59813090—
Product4-(Dibenzylamino)-6-methoxy-1-naphthaldehydeHCID 5981311798%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 4 (17.88 g, 43 mmol) and 10% aqueous sodium hydroxide solution (860 mL) in tetrahydrofuran (500 mL) was stirred at 50° C. for 5 days. The mixture was cooled to 0° C. and neutralized with concentrated hydrochloric acid. The mixture was concentrated under reduced pressure, and the product was extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and concentrated to give tert-butyl 4-bromo-7-hydroxynaphthalen-1-ylcarbamate (5). (14.32 g, 98% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435752B2
Source datasetuspto-grants-2008_10
ORD IDord-94cfd5f1fa4445ec928962fdec42f1ee
Source noteuspto-grants-2008_10