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HRID 434721作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl IsocyanateHCID 12228—
反応物4-(2-Hydroxybenzylideneamino)-1-naphtholHCID 135689608—
触媒Di-n-butyl diacetoxy tinHCID 9798523—
溶媒TetrahydrofuranHCID 8028—
生成物4-(2-Hydroxybenzylideneamino)naphth-1-yl methylcarbamateHCID 135689617100%

反応手順

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##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04399148
出典データセットuspto-grants-1983_08
ORD IDord-877c77b0d6394bb6abe197c36150f87d
出典メモuspto-grants-1983_08