Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1(3H)-Isobenzofuranone, 3-bromo- | HCID 96218 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | HCID 178453624 | HCID 178453624 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178479227 | HCID 178479227 | — |
Reaction Steps
A solution of 3-bromophthalide (70.5 g; 0.33 mol) in dimethylformamide (65 ml) was added dropwise to a cold solution of trans-4-(tert.-butyloxycarbonylaminomethyl) cyclohexanecarboxylic acid (77.1 g; 0.3 mol) in triethylamine (36.4 g; 0.36 mol) and dimethylformamide (195 ml). After 18 h the solvent was evaporated, water (1.5 L) and ethyl acetate (1.5 L) were added. The ethyl acetate extract was washed, dried and evaporated to give 122 g. This was dissolved in ethyl acetate (400 ml) and ethyl acetate/hydrochloric acid was added at ice bath temperature. After 2 h at room temperature, the precipitate was filtered, washed and dried to yield 63.8 g. This substance was dissolved in methanol, filtered through charcoal and precipitated with diethyl ether. Yield 54.4 g (56%), m.p. 212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04483867 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-5719f68089394248a48c7127abdbc39f |
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| Source note | uspto-grants-1984_11 |
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