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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435403Generated: October 28, 2026

Tetrahydrofuran → HCID 13091049, compound

https://huagongshe.com/reaction/435403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantL-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)-HCID 90234—
ReactantO-BENZYL-L-SERINE METHYL ESTER HYDROCHLORIDEHCID 44630138—
SolventDimethylformamideHCID 6228—
ProductHCID 13091049HCID 13091049875.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

THF (700 ml) and BOC-Ser(Bzl)-OH (23.6 g, 0.8 M) and HOBT (108 g, 0.8 M) were added to H-Ser(Bzl)-Ome.HCl (196.57 g, 0.8 M); and DMF (200 ml) was added to prepare a solution. WSCI (146 ml, 0.8 M) was added dropwise thereto at 0° C. and the mixture was stirred at 0° C. for one hour and at room temperature overnight. The reaction mixture was concentrated in vacuo, and ethyl acetate (1 l.) was added to the residue, which was then washed with 5% sodium bicarbonate solution, 1 N HCl and water, each three times, in that order. Hexane was added to the oily product, which was then crystallized by adding crystalline seed. The material was then recrystallized from ether-hexane to obtain the substance [28] (340.4 g, yield: 87.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04400316
Source datasetuspto-grants-1983_08
ORD IDord-3fca5602cd2b43a4b2574f7af368fe6d
Source noteuspto-grants-1983_08