HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917493Generated: October 27, 2026
Benzoyl isothiocyanate → tert-butyl N-[(4-{[(benzoylamino)carbothioyl]amino}cyclo-hexyl)methyl]carbamate
https://huagongshe.com/reaction/917493
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 1,1-Dimethylethyl N-((4-aminocyclohexyl)methyl)carbamate | HCID 21882540 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl N-[(4-{[(benzoylamino)carbothioyl]amino}cyclo-hexyl)methyl]carbamate | HCID 15524265 | 91.2% |
Reaction Steps
A solution of tert-butyl N-[(4-aminocyclohexyl)methyl]carbamate (4.683 g, 20.5 mmol) and benzoyl isothiocyanate (3.77 g, 23.1 mmol) in 180 ml THF was stirred at room temperature for 20 hours. The solvent was removed in vacuo to yield a golden viscous oil. The oil was triturated with 250 ml hexane and the resulting solid was collected by filtration and washed with hexane. The off-white solid was washed several times with hexane and was dried under vacuum to yield 91% (7.32 g) of the desired product as an off-white solid: 1H-NMR (CDCl3) δ 1.20 (6H, m), 1.44 (9H, s), 1.83 (2H, m), 2.25 (2H, m), 3.01 (2H, t, J=6.4 Hz), 4.20 (1H, m), 4.62 (1H, m), 7.51 (2H, t, J=7.9 Hz), 7.60 (1H, t, J=7.4 Hz), 7.81 (2H, d, J=7.2 Hz), 8.93 (1H, s); 392 (ESMS, MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07273880B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-6a5154e9f0c94fa89dfc40dc78edaea4 |
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| Source note | uspto-grants-2007_09 |
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