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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156952Generated: October 31, 2026

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

https://huagongshe.com/reaction/1156952

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 sulfate. 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 +12.5° (c=0.67, DMF).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04337247
Source datasetuspto-grants-1982_06
ORD IDord-0bca650f6b8d44deb938267694ab8697
Source noteuspto-grants-1982_06