Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromopropylamine hydrobromide | HCID 78701 | — |
| Reactant | Isocyanatocarbonyl chloride | HCID 119708 | — |
| Product | HCID 57266132 | HCID 57266132 | — |
Reaction Steps
To 3-bromo-1-propylamine hydrobromide (1.0 g, 4.56 mmol) in THF (20 mL) was added triethylamine (2.31 g, 22.8 mmol). The mixture was cooled to -78° C., triturated with N-(chlorocarbonyl)isocyanate (723 mg, 6.85 mmol) and stirred for 10 min. It was then concentrated, and the residue was partitioned between EtOAc and water. The organic layer was dried over Na2SO4, filtered and concentrated to give, in quantitative yield, the crude product which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046331 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-1c5bc66c5e8349f7bde5df428ff0b3b3 |
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| Source note | uspto-grants-2000_04 |
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