HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Iodo-4-methylthiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 3-iodo-4-methylthiophene-2-carboxylate | HCID 2761204 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Iodo-4-methylthiophene-2-carboxylic acid | HCID 2761391 | 100.1% |
Reaction Steps
To a solution of methyl 3-iodo-4-methylthiophene-2-carboxylate [Oakwood Product Inc.] (10 g, 35.4 mmol) in THF (200 mL) was added a solution of 2N NaOH (19.50 mL, 39.0 mmol). MeOH was added to the reaction mixture until a homogeneous solution was obtained. After about 4 h, concentrated HCl was added until a pH of about 1 was obtained. The reaction mixture was partially concentrated under reduced pressure and the resulting solid was collected by filtration and dried under reduced pressure to provide the title compound as a brown solid (9.50 g, 100%): LC/MS (Table 1, Method a) Rt=2.55 min; m/z: 267 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101645B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-2ab90379767a459f929aa5959fa81b6a |
| Source note | uspto-grants-2012_01 |