Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | n-Heptyl isocyanate | HCID 138341 | — |
| Reactant | HCID 20086779 | HCID 20086779 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9889686 | HCID 9889686 | — |
Reaction Steps
A solution of the product from step (d) (4.5 g) in THF (50 ml) was stirred at room temperature and heptyl isocyanate (5.5 g containing 36 mole % benzene, prepared by the method described in Organic Syntheses, Collective Volume 3, p. 846) and N,N-dimethylaminopyridine (750 mg) were added. The mixture was stirred at room temperature for ca 60 hours, then evaporated under reduced pressure to give an oil which was flash chromatographed through a silica column using ether/hexane (2:1 v/v). The eluate was evaporated under reduced pressure and the residue crystallised from hexane and triturated with methanol to give 4.5 g of material. The latter was flash chromatographed through a silica column using ether/hexane (2:1 v/v) and then freeze-dried from dioxan to give 5.3 g of the desired product, mp 105°-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05290814 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-da026529a68d4f8bb97de824a4be1d09 |
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| Source note | uspto-grants-1994_03 |
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