HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47745Generated: October 26, 2026
tert-Butyl isothiocyanate → N-[(2S)-2-hydroxypropyl]-N'-tert-butylthiourea
https://huagongshe.com/reaction/47745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl isothiocyanate | HCID 11544 | — |
| Reactant | (S)-(+)-1-Aminopropan-2-ol | HCID 7311736 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[(2S)-2-hydroxypropyl]-N'-tert-butylthiourea | HCID 23381537 | 93.6% |
Reaction Steps
The process is performed as in Example 1, starting with 5 g of (+)-(S)-1-amino-2-propanol and 8.43 g of tert-butyl isothiocyanate in 60 cm3 of ethanol. After stirring the reaction medium for 5 hours at a temperature in the region of 20° C. and then concentration under reduced pressure (5 kPa) at a temperature in the region of 50° C., the white solid obtained is taken up in diethyl ether. The suspension is again concentrated under the same conditions as above. 11.86 g of N-[(2S)-2-hydroxypropyl]-N′-tert-butylthiourea are obtained in the form of a white solid melting at 106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06699895B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-7e98585b952d43d2904d99276cac5898 |
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| Source note | uspto-grants-2004_03 |
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