HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (7-Iodo-4-methoxy-benzothiazol-2-yl)-carbamic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (4-Methoxy-benzothiazol-2-yl)-carbamic acid methyl ester | HCID 21303403 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (7-Iodo-4-methoxy-benzothiazol-2-yl)-carbamic acid methyl ester | HCID 60117385 | — |
Reaction Steps
(4-Methoxy-benzothiazol-2-yl)-carbamic acid methyl ester (31.0 g, 130 mmol) and sodium acetate (32.3 g, 394 mmol) are dissolved in 400 ml of glacial acetic acid and slowly treated with iodine monochloride (13.5 ml, 264 mmol) at 0° C. The reaction mixture is then slowly warmed to room temperature and stirred for 15 hours. After addition of water (1.31), the formed precipitate is filtered off and washed with water. The filter cake is then dissolved in a minimal amount of tetrahydrofurane (about 150 ml) and decolorized with 1M aqueous sodium thiosulfate. The product is precipitated by the addition of water (about 2.0 l), filtered off and dried at 60° C. for 12 hours. 42.3 g (89%) white solid. MS: m/e=364 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06963000B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-63af70d7b9354733b2ab2b3e3911b62b |
| Source note | uspto-grants-2005_11 |