HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Isopropylaniline → 4-Iodo-2-(propan-2-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Isopropylaniline | HCID 12561 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Iodo-2-(propan-2-yl)aniline | HCID 12667938 | — |
Reaction Steps
Iodine monochloride (12.9 cm3) was added at room temperature to a stirred solution of 2-[prop-2-yl]-aniline (27.0 g) and sodium acetate (16.4 g) in acetic acid (250 cm3). After 1 hour, volatile material was removed in vacuo and the residue was partitioned between ethyl acetate (200 cm3) and 10% sodium carbonate solution (50 cm3). The dried (MgSO4) organic extract was filtered and evaporated in vacuo to afford an oil which was chromatographed on silica (Merck "MK 60.9385") eluting with hexane. Combination and evaporation of the product containing fractions gave the product as a crude dark unstable oil (38 g) which was not characterised fully but was used directly in Preparation 84.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04710507 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-6a071a4aec4d4fd0a48892b03475ad72 |
| Source note | uspto-grants-1987_12 |