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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106300Generated: October 30, 2026

Trifluoroacetic acid → HCID 131712661, compound

https://huagongshe.com/reaction/1106300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dioneHCID 89529—
ReactantBoc-Met(O)-OhHCID 7408090—
ReactantHCID 131711783HCID 131711783—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131712661HCID 131712661—

Reaction Steps

To 50.0 g of Boc-Asn-Thr-OBzl is added 170 ml of TFA and the mixture is shaken at room temperature for 30 minutes. The solution is concentrated and treated with 500 ml of diethyl ether. The resultant powder is collected by filtration and dried. It is dissolved in 400 ml of THF, and under ice-cooling 20 ml of TEA is added. To this solution is added Boc-Met(O)-ONB (prepared by dissolving 31.3 g of Boc-Met(O).OH and 23.3 g of HONB in 200 ml of THF, adding 26.8 g of DCC under ice-cooling and stirring the mixture for 4 hours). The mixture is stirred for 15 hours, after which time the solvent is distilled off under reduced pressure. To the residue are added ethyl acetate (200 ml) and ether (200 ml), and the resultant powders are collected by filtration and reprecipitated from acetonitrile. Yield 48.5 g (72.0%), m.p. 145°-147° C., [α]D23 -6.5° (c=1.1, DMF), Rf1 =0.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04312943
Source datasetuspto-grants-1982_01
ORD IDord-0c03792db83547caa4a55fd3570e1609
Source noteuspto-grants-1982_01