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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434721Generated: October 24, 2026

Methyl Isocyanate → 4-(2-Hydroxybenzylideneamino)naphth-1-yl methylcarbamate

https://huagongshe.com/en/reaction/434721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
Reactant4-(2-Hydroxybenzylideneamino)-1-naphtholHCID 135689608—
CatalystDi-n-butyl diacetoxy tinHCID 9798523—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Hydroxybenzylideneamino)naphth-1-yl methylcarbamateHCID 135689617100%

Reaction Steps

To a 350 milliliter glass pressure bottle equipped with a magnetic stirrer was added 4.00 grams (0.015 moles) of 4-(2-hydroxybenzylideneamino)-1-naphthol prepared in Part A, 1.03 grams (0.018 moles) of methyl isocyanate, 100 milliliters of tetrahydrofuran and 5 drops of dibutyl tin diacetate. The resulting reaction mixture was stirred for 18 hours at room temperature after which the volatiles were removed under reduced pressure and the remaining residue dissolved in ether. The ethereal solution was washed twice with a 1% aqueous sodium bicarbonate solution and twice with a saturated brine solution, dried over magnesium sulfate and concentrated under reduced pressure to give 4.87 grams (0.015 moles) of 4-(2-hydroxybenzylideneamino)naphth-1-yl methylcarbamate in the form of a pale yellow solid having a melting point of 143°-145.5° C. and the following structural formula: ##STR16##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399148
Source datasetuspto-grants-1983_08
ORD IDord-877c77b0d6394bb6abe197c36150f87d
Source noteuspto-grants-1983_08