HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280646Generated: October 31, 2026
tert-Butyl isothiocyanate → N-(tert-butyl)-N'-[(1S)-1-cyclohexylmethyl-2-hydroxyethyl]thiourea
https://huagongshe.com/reaction/1280646
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl isothiocyanate | HCID 11544 | — |
| Reactant | (2S)-2-amino-3-cyclohexylpropan-1-ol | HCID 444569 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(tert-butyl)-N'-[(1S)-1-cyclohexylmethyl-2-hydroxyethyl]thiourea | HCID 86584434 | — |
Reaction Steps
The process is performed as in Example 3, starting with 8.1 g of (+)-(2S)-2-amino-3-cyclohexyl-1-propanol and 9.8 cm3 of tert-butyl isothiocyanate in 79 cm3 of ethanol. The reaction medium is stirred for 72 hours at a temperature in the region of 20° C. After concentration of the reaction mass under reduced pressure (5 kPa) at a temperature in the region of 50° C., the oil obtained is taken up in 110 cm3 of cold petroleum ether. The crystals are filtered off and dried under reduced pressure (10 Pa) at a temperature in the region of 60° C. 11.1 g of N-(tert-butyl)-N′-[(1S)-1-cyclohexylmethyl-2-hydroxyethyl]thiourea are obtained in the form of a white solid melting at 97° C.
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-0accdeeece8740549a7a2e6dba6dbd87 |
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| Source note | uspto-grants-2002_09 |
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