Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Diisocyanatobenzene | HCID 61009 | — |
| Reactant | 3-Methylbut-1-yne | HCID 69019 | — |
| Reactant | HCID 57535331 | HCID 57535331 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57535349 | HCID 57535349 | 72.1% |
Reaction Steps
To a solution of (1-Ethyl-3-nitro-2-trimethylsilanyloxy-propyl)-carbamic acid tert-butyl ester (918 mg, 2.86 mmol), 1,4-Phenylene diisocyanate (1.38 g, 8.5 mmol) and 3-methyl-1-butyne (586 mg, 8.5 mmol) in dry toluene (15 mL) under N2 is added triethylamine (10 drops). The mixture is heated to 50° C. in a sealed vial for 28 h, and then cooled to room temperature Water (1 mL) is added and the mixture is stirred for an additional 2 h, then filtered. The filtrate is concentrated in vacuum and the residue is purified over 35 g silica gel, eluted with ethyl acetate: heptane (1:5) to afford {1-[(5-Isopropyl-isoxazol-3-yl)-trimethylsilanyloxy-methyl]-propyl}-carbamic acid tert-butyl ester (764 mg, 72%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482448B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-d029dcc7bd4a430dab5e7ea47d9c7f02 |
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| Source note | uspto-grants-2009_01 |
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