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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554819Generated: October 31, 2026

Methanesulfonic Acid → HCID 67458340, compound

https://huagongshe.com/reaction/554819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
Reactant2,4,6-TrimethoxybenzaldehydeHCID 70019—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(2S)-3-[(tert-butoxycarbonyl)amino]-2-(5-chloro-2-methoxybenzyl)propanoic acidHCID 66935162—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 67458340HCID 67458340—

Reaction Steps

(2S)-3-[(tert-butoxycarbonyl)amino]-2-(5-chloro-2-methoxybenzyl)propionic acid (10g) was dissolved in ethyl acetate (120 ml), then methane sulfonic acid (9.4 ml) was added at room temperature, and the resulting mixture was stirred at that temperature for 2 hours. To the reaction solution was added triethylamine (20.3 ml), and the mixture was stirred for 13 hours. Then 2,4,6-trimethoxybenzaldehyde (5.7 g) was added and the mixture was stirred for 30 minutes. Next, to the reaction solution, sodium triacetoxyborohydride (9.3 g) was added and the mixture was stirred for 2 hours. To the reaction solution, a 1N aqueous sodium hydroxide solution was added, and the layers were separated. The aqueous layer was extracted again with ethyl acetate. The organic layer was washed with a 1N aqueous sodium hydroxide solution, then the appeared precipitated crystals were collected by filtration and dried to obtain the title compound (11.5 g) as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049006B2
Source datasetuspto-grants-2011_11
ORD IDord-a936a41559074d77bac253747f5ebdbc
Source noteuspto-grants-2011_11