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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993738Generated: October 31, 2026

Hexane → N-({[1-ethyl-1-(hydroxymethyl)propyl]amino}carbonothioyl)benzamide

https://huagongshe.com/reaction/1993738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantBenzoyl isothiocyanateHCID 68284—
Reactant2-Amino-2-ethylbutan-1-olHCID 14325607—
SolventTetrahydrofuranHCID 8028—
ProductN-({[1-ethyl-1-(hydroxymethyl)propyl]amino}carbonothioyl)benzamideHCID 8661857980.1%

Reaction Steps

Benzoyl isothiocyanate (4.28 mL, 31.8 mmol) was added under nitrogen to a solution of 2-amino-2-ethylbutan-1-ol (3.7315 g, 31.8 mmol), prepared in the previous step, in 100 mL of anhydrous tetrahydrofuran (exotherm on addition). After the addition, the reaction was refluxed for 2.5 h. After cooling to room temperature, 100 mL of hexane was added. The solid that formed was collected by filtration and dried under reduced pressure to give N-({[1-ethyl-1-(hydroxymethyl)propyl]amino}carbonothioyl)benzamide (7.1406 g, 80%) as a white solid, mp 161-163° C.; MS (ESI) m/z 281 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652018B2
Source datasetuspto-grants-2010_01
ORD IDord-095ffc4dffe04b6c86f1938e253d9558
Source noteuspto-grants-2010_01