HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068529Generated: October 31, 2026
Aminoacetaldehyde dimethyl acetal → HCID 178495874, compound
https://huagongshe.com/reaction/2068529
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | Benzyl N-(2-thioxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl)carbamate | HCID 58304049 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178495874 | HCID 178495874 | 118% |
Reaction Steps
Dissolve Benzyl N-(2-thioxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl)carbamate (1.78 Kg, 5.13 mol) and para-toluene sulfonic acid monohydrate (48.8 g, 256 mmol) in dichloromethane (12 L). Add aminoacetaldehyde dimethyl acetal (2.70 Kg, 25 mole) dropwise over 1 hour and stir for 36 hours at ambient temperature. Add additional aminoacetaldehyde dimethyl acetal (1.40 Kg, 13 mol) and stir for 12 hours at ambient temperature. Add water (5.0 L), separate the organic layer, and extract the aqueous with dichloromethane (2.0 L). Combine the organic layers and wash with water, saturated ammonium chloride (6.0 L), and brine (4.0 L). Filter the organic through diatomaceous earth and concentrate under reduced pressure to give the title compound (2.30 kg, 118%) as a yellow oil: MS (m/z): 398 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299061B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-9d666702616e4100907991979644d9ed |
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| Source note | uspto-grants-2012_10 |
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