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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968963Generated: October 27, 2026

Formic Acid → For-Orn(Z)-OH

https://huagongshe.com/reaction/968963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
ReactantH-Orn(Z)-OHHCID 7009570—
SolventWaterHCID 962—
ProductFor-Orn(Z)-OHHCID 1166648288%

Reaction Steps

444.7 g (1.67 mole) of commercially available H—Orn(Z)—OH was dissolved in 3.5 L (93 moles) of formic acid. The solution was cooled in an ice bath, and 1.17 L (12 moles) of acetic anhydride was subsequently added in dropwise fashion over two hours while the temperature of the reaction mixture was maintained between about 5° and 15° C. The resultant reaction mixture was stirred at room temperature for about two hours after the addition was completed, and the reaction vessel was refrigerated overnight. 1.5 L of cold water was then added, and the solution was concentrated to dryness under reduced pressure. The residual, light yellow syrup was taken up into EtOAc, washed with water and then with saturated NaCl, and then dried overnight over sodium sulfate. After filtration and evaporation to dryness, the residual syrup was dissolved in 5 L of ethyl ether. The solution was cooled in a dry ice bath and seeded. The resulting crystalline product was filtered, washed with ethyl ether, air dried for two hours and finally dried in a lyophilizer. 431.6 g (1.47 mole, 88%) of For—Orn(Z)—OH was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304181B2
Source datasetuspto-grants-2007_12
ORD IDord-bec49be841e6491c86e16b0cbcc4fc55
Source noteuspto-grants-2007_12