Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 77975665 | HCID 77975665 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86739452 | HCID 86739452 | 94.2% |
Reaction Steps
4-Allyloxy-3-chloro-phenylacetyl-(DL)-alanine methyl ester (2.0 g) was suspended in acetone (20 ml). Aqueous sodium hydroxide (1M, 8.0 ml) was added and the mixture was gently warmed to effect solution, and then heated at 40° C. for 20 min. After the solution has been cooled, the pH was adjusted to 2-3 using dilute hydrochloric acid (3M) and the product was extracted with ethyl acetate (40 ml). The extract was dried (anhydrous sodium sulphate). The solvent was evaporated at reduced pressure to leave a solid residue (1.8 g); it had m.p. 120°-124° C. After recrystallisation from ethyl acetate/light petroleum (b.p. 60°-80° C.) the above-named product, (1.6 g), m.p. 123°-124° C. was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04505898 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-6e67418ecf7a4ee9a97df28a017ae0c2 |
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| Source note | uspto-grants-1985_03 |
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