Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylamine | HCID 7582 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Cd 394 | HCID 3086541 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54115622 | HCID 54115622 | — |
Reaction Steps
2.0 g (5 mmoles) of 4-[3-(1-adamantyl)-4-methoxy benzamido]benzoic acid are dissolved in 60 ml of THF. 1.1 g (6 mmoles of dicyclohexylamine are slowly added. A white precipitate is immediately formed. The reaction mixture is then cooled to 0° C. and 0.7 g (6 mmoles) of thionyl chloride is slowly added. The reaction mixture is stirred for 3 hours at ambient temperature. The solid that forms is filtered and then the filtrate is evaporated. The resulting residue is used, as is, in the following synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04927928 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-22c70c46ae6943029bd25f5a458d8979 |
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| Source note | uspto-grants-1990_05 |
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