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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075128Generated: November 1, 2026

Camphor → HCID 20398731, compound

https://huagongshe.com/reaction/1075128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCamphorHCID 2537—
Reactant1-NaphthylamineHCID 8640—
Reactant1-Naphthalenamine, hydrochloride (1:1)HCID 11094—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductHCID 20398731HCID 20398731—

Reaction Steps

Camphor (10 gm), 9.4 gm α-naphthylamine, 0.1 gm α-naphthylamine-HCl and 30 gm 1 A molecular sieves were added to 40 ml anhydrous methanol. Sodium cyanoborohydride (2.5 gm) was added dropwise and stirred under N2 for 48 hours. The sieves were removed by filtration and 5 drops of concentrated HCl were added to the filtrate until it was acidic (pH>7). The solvent was stripped by boiling and 10 gm potassium hydroxide was added to the remaining mixture. The aqueous phase was extracted with ether over potassium carbonate. The extractions were filtered to remove the potassium carbonate. After the ether was evaporated, the mixture was distilled under high vacuum. The material boiling at 120° C. and 0.1 mm of mercury was collected. IR spectra verified that this material was the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04394070
Source datasetuspto-grants-1983_07
ORD IDord-ae224df24e8548bc8b0ba8d6455a3429
Source noteuspto-grants-1983_07