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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443922Generated: October 25, 2026

Ethylmorpholine → Boc-MePhe methioninol

https://huagongshe.com/reaction/443922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
ReactantIsobutyl chloroformateHCID 62365—
ReactantL-MethioninolHCID 2724404—
ReactantBoc-N-Me-Phe-OHHCID 7010602—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductBoc-MePhe methioninolHCID 131712176—

Reaction Steps

3.1 g of Boc-MePhe-OH are dissolved in 30 ml of tetrahydrofuran, cooled to -20°, and 1.45 ml of N-ethylmorpholine are added with stirring followed by 1.45 ml of chloroformic acid iso-butyl ester and the mixture stirred for a further 5 minutes at -20°. A cold solution of 1.80 g of methioninol in 1 ml of tetrahydrofuran is added, the mixture left to stand for 2 hours at a temperature of from -5° to 0° and then stirred for 2 hours at room temperature. The reaction mixture is diluted with ca. 350 ml of acetic acid and washed repeatedly with water, 1 N citric acid, 10% KHCO3 and 30% NaCl solution. The organic phase is dried over Na2SO4 and evaporated, whereby Boc-MePhe-methioninol is obtained as an amorphous product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261888
Source datasetuspto-grants-1981_04
ORD IDord-a177efbe882b49f99b0a5f2d55b737f4
Source noteuspto-grants-1981_04