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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744421Generated: October 30, 2026

Methanesulfonic Acid → HCID 86605368, compound

https://huagongshe.com/reaction/1744421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantMethyl 3-aminocrotonateHCID 643918—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
ProductHCID 86605368HCID 8660536861.3%

Reaction Steps

Under a nitrogen atmosphere, 78.0 mg (0.0869 mmol) of Ru(OCOCH3)2((R)-tol-binap), 1.00 g (8.69 mmol) of methyl 3-aminocrotonate, 0.83 g (8.69 mmol) of methanesulfonic acid and 5 ml of methanol were placed in a stainless steel autoclave, and the mixture was kept at 50° C. under 3MPa pressure of hydrogen for 15 hours with stirring. After completion of the reaction, the solvent was distilled off, and the residue was recrystallized from methanol/ethyl acetate to give the objective methyl (R)-3-aminobutanoate methanesulfonate (1.135 g, white crystals). The yield was 61.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015348B2
Source datasetuspto-grants-2006_03
ORD IDord-6dd9b501d4b74a9f922a30740069649c
Source noteuspto-grants-2006_03