Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352280Generated: October 31, 2026

p-Toluenesulfonic acid monohydrate → HCID 14601401, compound

https://huagongshe.com/reaction/2352280

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 14601400HCID 14601400—
SolventAcetoneHCID 180—
ProductHCID 14601401HCID 1460140191.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876271
Source datasetuspto-grants-1989_10
ORD IDord-bbbda4c4cda14f07ba242de27798665b
Source noteuspto-grants-1989_10