HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 3-Tert-butyl-4-hydroxy-5-iodobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3-(tert-Butyl)-4-hydroxybenzaldehyde | HCID 3017618 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Catalyst | Sodium Pyrosulfite | HCID 656671 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Tert-butyl-4-hydroxy-5-iodobenzaldehyde | HCID 18677384 | 131.4% |
Reaction Steps
A slurry of 3-tert-butyl-4-hydroxybenzaldehyde (16 gm) sodium hydroxide (3.5 gm), potassium iodide (10.3 gm), potassium in distilled water (91 ml) was added dropwise during 20 mins to a stirred solution of ethanol (69 ml), water (15 ml) and and concentrated sulphuric acid (7.5 ml) at 50°-55° C. After addition, the mixture was refluxed for 1 hour. Sodium metabisulphite (1 gm) was added to the mixture and on cooling a precipitate formed. The precipitate was collected and recrystallised from petroleum ether to give 3-tert-butyl-4-hydroxy-5-iodobenzaldehyde (24.8 gm) m.p. 124°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064266 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-d830b619a9db46d7bc115f370cd80d0c |
| Source note | uspto-grants-1977_12 |