HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280643Generated: October 25, 2026
tert-Butyl isothiocyanate → N-(tert-butyl)-N'-[(1R)-1-butyl-2-hydroxyethyl]thiourea
https://huagongshe.com/reaction/1280643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl isothiocyanate | HCID 11544 | — |
| Reactant | (R)-2-Aminohexan-1-ol | HCID 6994402 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(tert-butyl)-N'-[(1R)-1-butyl-2-hydroxyethyl]thiourea | HCID 86584433 | — |
Reaction Steps
The process is performed as in Example 2, starting with 1.14 g of (2R)-2-amino-2-butyl-1-ethanol and 1.36 cm3 of tert-butyl isothiocyanate in 15 cm3 of ethanol, with stirring for 18 hours at a temperature in the region of 20° C. and then for 3 hours in the region of 60° C. After concentration of the reaction medium under reduced pressure (5 kPa) at a temperature in the region of 40° C. 2.38 g of N-(tert-butyl)-N′-[(1R)-1-butyl-2-hydroxyethyl]thiourea are obtained in the form of a yellow oil. Infrared spectrum (CH2Cl2): 3620; 4430; 4410; 2960; 1560; 1500; 1395; 1375 and 1205 cm−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451821B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-b44fe8087a774d4e8311a5d17e1c76e2 |
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| Source note | uspto-grants-2002_09 |
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