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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277393Generated: November 1, 2026

Tetrahydrofuran → Ethyl (tert-butoxycarbonyl)-D-methionylglycinate

https://huagongshe.com/reaction/1277393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dioneHCID 89529—
ReactantN-(tert-Butyloxycarbonyl)-D-methionineHCID 111051—
ProductEthyl (tert-butoxycarbonyl)-D-methionylglycinateHCID 12919642—

Reaction Conditions

Temperature0 °C

Reaction Steps

In 100 ml of THF are dissolved 10.0 g of BOC-(D)-Met-OH and 7.9 g of HONB, followed by cooling at 0° C. and adding 9.0 g of DCC, and the mixture is stirred at 0° C. for 6 hours. Insoluble matters are filtered out, and 5.9 g of H-Gly-OEt·HCl salt and 5.6 ml of TEA are added to the filtrate, which is then stirred overnight at room temperature. The THF is distilled off and the residue is extracted with 100 ml of AcOEt, followed by washing with water and drying over anhydrous sodium sulphate. The AcOEt is distilled off and the residue is crystallized with petroleum ether. Recrystallization from AcOEt-petroleum ether yields 9.8 g of the desired product, m.p. 55°-56° C., Rf1 =0.70, [α]D21 +2.5° (c=0.67, DMF)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04277394
Source datasetuspto-grants-1981_07
ORD IDord-71976bd1ebbc4054ac36f74a196b4d1f
Source noteuspto-grants-1981_07