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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684402Generated: October 30, 2026

Water → Boc-beta-chloro-ala-oh

https://huagongshe.com/reaction/1684402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
Reactant3-chloro-L-alanineHCID 439772—
Solvent1,4-DioxaneHCID 31275—
ProductBoc-beta-chloro-ala-ohHCID 702077047.2%

Reaction Steps

To a solution of 1.0 g (6.25 mmol) of 3-chloro-L-alanine and 1.3 mL of triethylamine in 50% aqueous 1,4-dioxane were added 1.69 g (6.90 mmol) of 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile with stirring at room temperature. After 2 hours, the reaction mixture was poured into 20 mL of water and extracted twice with ethyl acetate. The organic layer was washed twice with water and then with saturated brine, dried over anhydrous magnesium sulfate and evaporated to give 0.66 g (40.5%) of white solid. Recrystallization from a mixture of ethyl acetate and n-hexane afforded 0.58 g of the pure product (35.6%) melting at 123°-124° C., with decomposition, and having the structural formula: ##STR55## The identity of the product was confirmed by IR and NMR analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639885
Source datasetuspto-grants-1997_06
ORD IDord-ded984cfa90d424fbdecc38d2378b033
Source noteuspto-grants-1997_06