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HRID 1375750作成日:2026年10月27日

Sodium Hydroxide → 1-(3-Methoxybenzyl)-3-Octadecyl Thiourea

https://huagongshe.com/reaction/1375750

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物OctadecylamineHCID 15793—
反応物3-Methoxybenzyl isothiocyanateHCID 126512—
反応物Stearamine hydrochlorideHCID 519552—
反応物HCID 178418790HCID 178418790—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物1-(3-Methoxybenzyl)-3-Octadecyl ThioureaHCID 12082055—

反応条件

温度4 °C

反応手順

Octadecyl amine hydrochloride was converted to the amine by mixing an ether solution of the amine hydrochloride with 1 M NaOH, separating and evaporating the ether layer, dissolving the amine in CHCl3, filtering through Whatman 541 filter paper and evaporating the CHCl3. Octadecyl amine (5.9252 g, 22.0 mmol) in 150 ml ethanol was reacted with an excess (4.32 g, 24.1 mmol) of 3-methoxybenzyl isothiocyanate at 40° C. under N2 with stirring. Excess isothiocyanate was used because co-crystallization of octadecyl amine is difficult to prevent when an excess of amine is present. After 2 h the solution was cooled to 4° C., centrifuged at 10,000 rpm for 20 min and the precipitated crystals were washed with ethanol (20 ml). The combined supernatant and wash was evaporated to 20 ml total volume and then cooled to −10° C. to filter off a second batch of crystals. The supernatant was dried and 94.3% of reagents weight was recovered, 74.9%, or 7.40 g as 1-(3-methoxybenzyl)-3-(octadecyl) thiourea of about 76% purity based on the sulfur analysis. The octadecyl amine was difficult to separate from the thiourea by crystallization. Calculated elemental analysis of 1-(3-methoxybenzyl)-3-octadecyl thiourea: C, 72.27; H, 10.78; N, 6.24; S, 7.15. Found: C, 71.96; H, 11.00; N, 5.95; S, 5.46. A recrystallization from acetone/chloroform gave crystals with the composition: C, 72.37; H, 10.98; N, 6.13; S, 6.92.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07169815B2
出典データセットuspto-grants-2007_01
ORD IDord-3d58813736d741e88b0095e000f09a71
出典メモuspto-grants-2007_01