HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → HCID 14601401, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 14601400 | HCID 14601400 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 14601401 | HCID 14601401 | 91.3% |
Reaction Steps
5-(2-Dioxolanyl)thieno[3,2-b]thiophene-2-sulfonamide (10) 8.50 g (0.029 moles) was dissolved in 500 mL acetone at room temperature and 0.9 g p-toluenesulfonic acid monohydrate was added in one portion. After 5 hours at room temperature all starting material was consumed. The reaction was quenched with 125 ml saturated NaHCO3 solution and the acetone was stripped on a rotary evaporator. The resulting viscous mass was extracted with 3×300 mL ethyl acetate and these combined extracts were dried and stripped to give 6.55 g (91%) of 5-Formylthieno[3,2-b]thiophene-2-sulfonamide (11) as a tan solid, mp. 203°-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04876271 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-bbbda4c4cda14f07ba242de27798665b |
| Source note | uspto-grants-1989_10 |