Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13785343 | HCID 13785343 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14032420 | HCID 14032420 | — |
Reaction Steps
A sample of N-acetyl-3-acetoxy-5-p-chlorophenylpyrrole (16) (2.8 g; 0.01 mol) was deoxygenated for ten minutes with a stream of N2. The solids were then dissolved in deoxygenated methanol (30 mL) which was then chilled to -8° C. At once was added a cold deoxygenated solution of NaOH (1.6 g; 0.04 mol) in 20 mL H2O, which solution was then heated briefly at 15° C. and then immediately cooled to -5° C.; after 25 minutes the clear solution was treated with a cold deoxygenated solution of citric acid (4.2 g; 0.02 mol) in 15 mL H2O and the temperature rose briefly to 5° C. After 0.5 hour of stirring at -5° C. the solids were collected by filtration and washed with cold deoxygenated H2O. The pale green product was dried under vacuum at room temperature over P2O5 for several days (1.3 g; 68%); TLC Rf=0.19 (CHCl3 :EtOH, 9:1), IR (KCl) showed no evidence for C=0 adsorption.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04637979 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-a6b8c47de3664fada4127341a868d4b7 |
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| Source note | uspto-grants-1987_01 |
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