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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418009Generated: October 27, 2026

Hydrochloric Acid → 2-Amino-3-(2-vinylphenyl)propanoic acid

https://huagongshe.com/reaction/1418009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant2-(Bis-methylsulfonyl-methyleneamino)-1-(10,10-dimethyl-3,3-dioxo-3-thia-4-aza-tricyclo[5.2.1.0 1,5]dec-4-yl)-3-(2-vinyl-phenyl)-propan-1-oneHCID 54502708—
Product2-Amino-3-(2-vinylphenyl)propanoic acidHCID 18612515—

Reaction Steps

For example, the appropriate 2-(bis-methylsulfonyl-methyleneamino)-1-(10,10-dimethyl-3,3-dioxo-3-thia-4-aza-tricyclo[5.2.1.0 1,5]dec-4-yl)-3-(2-vinyl-phenyl)-propan-1-one derivative of structure (5) is treated with a suitable acid such as aqueous hydrochloric acid in a suitable organic solvent such as tetrahydrofuran. The reaction is conducted at a temperature range of from -10° C. to room temperature and for a period of time ranging from 30 minutes to 20 hours. Evaporation of the solvent followed by treatment with inorganic base such as aqueous lithium hydroxide in a suitable organic solvent, such as tetrahydrofuran. The reaction is conducted at a temperature range of from -10° C. to room temperature and for a period of time ranging from 30 minutes to 10 hours. After acidification, the corresponding 2-amino-3-(2-vinyl-phenyl)-propionic acid derivative of structure (6) was isolated by evaporation of solvents.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880119
Source datasetuspto-grants-1999_03
ORD IDord-35d59221969b412aba2fe7bf3900825c
Source noteuspto-grants-1999_03