HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378810Generated: October 26, 2026
1,1-Ethanediol → 6-Bromo-5,8-dimethylspiro[thiochromane-4,2'-[1,3]dioxolane]
https://huagongshe.com/reaction/378810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Ethanediol | HCID 151211 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 5,8-Dimethyl-6-bromothiochroman-4-one | HCID 15278495 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Trimethyl orthoformate | HCID 9005 | — |
| Product | 6-Bromo-5,8-dimethylspiro[thiochromane-4,2'-[1,3]dioxolane] | HCID 21696593 | — |
Reaction Steps
58.4 g (0.22 mol) of 6-bromo-5,8-dimethyl-4-thiochromanone were dissolved in 380 ml of trimethyl orthoformate, admixed with 555 g (8.9 mol) of ethanediol and 0.2 g of p-toluenesulfonic acid monohydrate and stirred at 80° C. overnight. The mixture was subsequently allowed to cool, diluted with 500 ml of diethyl ether and washed with a 1:1 mixture of 1 M aqueous sodium hydroxide solution and sat. NaCl solution (2×500 ml) and subsequently with sat. NaCl solution (300 ml). The organic phase was dried over MgSO4 and concentrated using a rotary evaporator. The residue was taken up in 50 ml of heptaneldiethyl ether (9:1) and stored in a cold place. The crystals which had precipitated overnight were filtered off with suction, washed with cold heptane and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06297196B1 |
|---|
| Source dataset | uspto-grants-2001_10 |
|---|
| ORD ID | ord-2d9e3ecf9bc24abbbd3d7d581b9c76a4 |
|---|
| Source note | uspto-grants-2001_10 |
|---|