HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904473Generated: October 29, 2026
Iodine → 2,4-Dimethyl-3-hydroxymethyl-5-iodothiophene
https://huagongshe.com/reaction/904473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | (2,4-Dimethylthiophen-3-yl)methanol | HCID 12875266 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2,4-Dimethyl-3-hydroxymethyl-5-iodothiophene | HCID 12875267 | — |
Reaction Steps
10.0 G. (46 mmol) of mercuric oxide and 14.7 g. (58 mmol) of iodine were added alternately over a period of 11/4 hrs. to a vigorously stirred solution of 8.2 g. (57.7 mmol) of 2,4-dimethyl-3-hydroxymethylthiophene in 300 ml. of benzene. The reaction mixture was kept at room temperature by cooling with an ice bath and stirring was continued for an additional hour. The mercuric iodide which precipitated was filtered and washed well with warm ethyl ether. The combined organic solutions were washed with 10% sodium thiosulfate and saturated sodium chloride solution, dried and evaporated. The resulting residue was dissolved in a minimum amount of hot ether, an equal amount of hexane was added and the solution cooled to -50° C. The crystals which precipitated were filtered and washed with cold hexane to yield after drying 2,4-dimethyl-3-hydroxymethyl-5-iodothiophene, m.p. 118.5°-120.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04230872 |
|---|
| Source dataset | uspto-grants-1980_10 |
|---|
| ORD ID | ord-2657eb006f02433891f96427cbb9cd5b |
|---|
| Source note | uspto-grants-1980_10 |
|---|