HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351917Generated: October 31, 2026
Acetaldehyde, 2,2-dimethoxy- → HCID 15523870, compound
https://huagongshe.com/reaction/351917
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde, 2,2-dimethoxy- | HCID 162650 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 14204091 | HCID 14204091 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 15523870 | HCID 15523870 | — |
Reaction Steps
To a suspension of 13.5 g of 5-aminobenzocyclobutane-1-carbonitrile in 400 ml of 1,2-dichloroethane there are added rapidly dropwise 26.5 ml of a 45% solution of 2,2-dimethoxyacetaldehyde in tert-butyl methyl ether, followed by 16 ml of acetic acid and then, in portions, 39.7 g of sodium triacetoxyborohydride. After increasing the temperature to 29° C., the reaction mixture is brought to ambient temperature, stirred for 1 hour 15 minutes and then hydrolysed by pouring the mixture into 500 ml of a saturated aqueous solution of NaHCO3. The organic phase is removed, washed with water, and concentrated under reduced pressure to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743818B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-36e31cdaa2f049b6bb3bcbba7d8a38df |
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| Source note | uspto-grants-2004_06 |
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