HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl isothiocyanate → N-(tert-butyl)-N'-[(1R)-2-hydroxy-1-(phenylmethyl)ethyl]thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl isothiocyanate | HCID 11544 | — |
| Reactant | phenylalaninol, (R)- | HCID 853475 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(tert-butyl)-N'-[(1R)-2-hydroxy-1-(phenylmethyl)ethyl]thiourea | HCID 86584424 | 98.8% |
Reaction Steps
The process is performed as in Example 2, starting with 5 g of (R)-(+)-2-amino-3-phenyl-1-propanol in 50 cm3 of ethanol and 5.7 g of tert-butyl isothiocyanate at a temperature in the region of 20° C. for 16 hours. After an identical work-up, 8.7 g of N-(tert-butyl)-N′-[(1R)-2-hydroxy-1-(phenylmethyl)ethyl]thiourea are obtained in the form of a white solid melting at 107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451821B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-a607c291800e4e6a8c4e5736e0569476 |
| Source note | uspto-grants-2002_09 |