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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090566Generated: October 26, 2026

Sodium Chloride → O-Benzyl-N-benzyloxycarbonyltyrosinol

https://huagongshe.com/reaction/1090566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantLithium ChlorideHCID 433294—
ReactantSodium borohydrideHCID 4311764—
Reactant0-benzyl-N-benzyloxycarbonyltyrosine methyl esterHCID 56982255—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductO-Benzyl-N-benzyloxycarbonyltyrosinolHCID 22863341199.8%

Reaction Steps

27.25 g of 0-benzyl-N-benzyloxycarbonyltyrosine methyl ester was dissolved in a mixed solvent of 185 ml of ethanol and 122 ml of tetrahydrofuran, and to the solution were added 5.8 g of lithium chloride and 5.2 g of sodium borohydride under ice cooling. The reaction mixture was stirred at a room temperature for 18 hours, and after the addition of 500 ml of saturated sodium chloride aqueous solution, extracted twice with 300 ml of chloroform. The extract was dried over magnesium sulfate and concentrated under a reduced pressure to obtain 25.4 g of the title compound as colorless crystals

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081246
Source datasetuspto-grants-1992_01
ORD IDord-008fda4f17e2455288691e97ce00afba
Source noteuspto-grants-1992_01