Multi-step Synthesis
A2 synthesis combines aliphatic and aromatic reactions. Key aromatic links: benzene → (conc. HNO₃/H₂SO₄) nitrobenzene → (Sn/HCl, NaOH) phenylamine → (NaNO₂/HCl < 10 °C) diazonium → (phenol/NaOH) azo dye, or (warm water) phenol. Benzene → (RCl/AlCl₃) alkylbenzene → (KMnO₄/OH⁻, heat) benzoic acid. Benzene → (RCOCl/AlCl₃) aryl ketone → (NaBH₄) secondary alcohol. Acyl chlorides make esters and amides. Plan by retrosynthesis, give reagents and conditions, and recognise each step's reaction type. Purify solids by recrystallisation and check purity by melting point.
Learning objectives
- Recall aromatic reaction routes.
- Plan syntheses of up to four steps.
- Name reaction types for each step.
- Describe purification and purity checks.
How could you make benzoic acid from benzene in two steps?
Core idea
A drug chemist starts with cheap benzene and ends with a medicine. Each step is a reaction you already know.
Put groups onto the ring by electrophilic substitution, then change them with familiar aliphatic chemistry. Fewer, higher-yield steps are better.
Key links between aromatic compounds.
Four steps: 90%, 80%, 75%, 60%. Overall yield?
- Goal
- %.
- Strategy
- Multiply.
- Two steps.
- All four.
Summary
- Ring first, side chain second.
- Give reagents, conditions, intermediates.
- Recrystallise and test melting point.
- Recrystallisation
- Purifying a solid by dissolving in hot solvent and cooling.
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