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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964712Generated: October 26, 2026

1-Naphthaldehyde → HCID 19077420, compound

https://huagongshe.com/reaction/964712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantBoron TrichlorideHCID 25135—
Reactant(4-Chloro-phenyl)-(neopentyl)-amineHCID 11424155—
SolventBenzeneHCID 241—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
ProductHCID 19077420HCID 1907742067.5%

Reaction Steps

A solution of (4-chloro-phenyl)-(neopentyl)-amine (6.58 g, 33.3 mmol) in benzene (15 mL) was added to a solution of boron trichloride (1.0 M in xylenes; 36.6 mL, 36.6 mmol) in benzene (40 mL) at 0° C. under a nitrogen atmosphere. Once the addition was complete, the resulting mixture was heated at reflux for 2 hours and then recooled to 0° C. A solution of 1-naphthaldehyde (5.72 g, 36.6 mmol, 5.0 mL), triethylamine (6.74 g, 66.6 mmol, 9.3 mL) and benzene (15 mL) was then added and the resulting mixture stirred 1 hour before diluting with ethyl acetate and aqueous 2N hydrochloric acid. The resulting mixture was shaken vigorously, the aqueous layer alkalized with aqueous 5N sodium hydroxide, and the layers separated. The aqueous layer was extracted with ethyl acetate (2×). The organic layers were combined, dried over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and purified by flash column chromatography (5:1 hexanes/ethyl acetate) to produce 7.95 g (67%) of the title compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05770594
Source datasetuspto-grants-1998_06
ORD IDord-02b3888dca4b4edd869ae38b606f252c
Source noteuspto-grants-1998_06