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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068529Generated: October 31, 2026

Aminoacetaldehyde dimethyl acetal → HCID 178495874, compound

https://huagongshe.com/reaction/2068529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantBenzyl N-(2-thioxo-1,3,4,5-tetrahydro-1-benzazepin-3-yl)carbamateHCID 58304049—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventDichloromethaneHCID 6344—
ProductHCID 178495874HCID 178495874118%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299061B2
Source datasetuspto-grants-2012_10
ORD IDord-9d666702616e4100907991979644d9ed
Source noteuspto-grants-2012_10