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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964788Generated: November 2, 2026

2-Pyridinecarboxaldehyde → HCID 178448296, compound

https://huagongshe.com/reaction/1964788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridinecarboxaldehydeHCID 14273—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantD-ValinolHCID 6950587—
SolventDichloromethaneHCID 6344—
ProductHCID 178448296HCID 178448296100%

Reaction Steps

Anhydrous MgSO4 (50 g, 415 mmol, 4.15 eq) and a substituted aryl or heteroaryl carboxaldehyde, e.g. 2-pyridinecarboxaldehyde (9.5 ml, 100 mmol, 1 eq), were added to a solution of (R)-(−)-2-amino-3-methyl-1-butanol (10.32 g, 100 mmol) in dry DCM (150 ml) at 0° C. The reaction was followed by LC/MS. The mixture was stirred at this temperature for 2 h 25. MgSO4 was filtered off and the DCM removed by evaporation to give the desired product (XVIII*), e.g. (2R)-3-methyl-2-{[(E)-2-pyridinylmethylidene]amino}-1-butanol as a yellowish oil (19.23 g, quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415480B2
Source datasetuspto-grants-2013_04
ORD IDord-13746ffd2cc84a8c80ce83e10cfddf3a
Source noteuspto-grants-2013_04