HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Butane sultone → HCID 59207798, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Butane sultone | HCID 15411 | — |
| Reactant | 63019-44-3 | HCID 298444 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59207798 | HCID 59207798 | 87% |
Reaction Steps
8.5 g (36.6 mmol) of N,N-dimethyl-4-[1,3-thiazol-2-yldiazenyl]aniline are heated with 85 ml of butane sultone at 110° C. for 6 hours. After cooling, 200 ml of tetrahydrofuran are added to the reaction mixture and the precipitated product is filtered off, washed with acetone and dried. The dye is recrystallized with methanol/ethyl acetate. 11.8 g (87% of theory) of 4-(2-{[4-(dimethylamino)phenyl]diazenyl}-1,3-thiazol-3-ium-3-yl)-1-butanesulfonate are obtained as a dark blue power.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393366B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-07e12ebad1c0464f8db6a0c195f5d008 |
| Source note | uspto-grants-2008_07 |