HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939852Generated: October 26, 2026
Aminoacetaldehyde dimethyl acetal → Benzene sulfonamido acetaldehyde dimethyl acetal
https://huagongshe.com/reaction/1939852
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | Benzene sulphochloride | HCID 22564087 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | Benzene sulfonamido acetaldehyde dimethyl acetal | HCID 3821256 | 101% |
Reaction Steps
56 g 2-aminoacetaldehyde dimethyl acetal are dissolved in 200 ml of a 14 wt. % aqueous sodium carbonate solution at 20 ° C. in a three-necked flask, equipped with a thermometer, reflux condenser, tap funnel and magnetic stirrer. Subsequently, 88 g benzene sulfochloride are added drop-wise within 1 hour at this temperature under intensive stirring followed by another 2 hours of heating the reaction to 40° to 50° C. mixture under vigorous stirring. After that the intensive smell of benzene sulfochloride has disappeared and a second phase has formed. This heavy oily phase is separated in the separatory funnel, imbibed using diethyl ether and dried over water-free sodium sulfate. Once the drying agent has been removed and the ether has been distilled off, 112 g of the product are obtained (yield: 88 based on the amino acetal used).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698360 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-0ae5ceb401a74070a80e1e70c4762bb6 |
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| Source note | uspto-grants-1997_12 |
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