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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416346Generated: November 1, 2026

HCID 86588600, compound → HCID 86588601, compound

https://huagongshe.com/reaction/2416346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86588600HCID 86588600—
SolventEthanolHCID 702—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 86588601HCID 86588601—

Reaction Steps

The N-t-butyloxycarbonyl-α-methyltyrosine methylester (1.70 g) from the previous synthesis was dissolved in 25 ml of absolute ethanol and treated with dry sodiun ethoxide (742 mg). 3-Bromopropanol (924 mg, 0.6 ml) was added and the solution was refluxed for 5 hours. The ethanol was then evaporated, 100 ml of dichloromethane added and the solution washed with 100 ml of water. After drying over MgSO4 the solvent was evaporated to yield two spots on a TLC plate developed in EtOAc:Hexane 1:1. The first spot was product and the second was starting material. The product was purified on a silica gel column using EtOAc:Hexane (1:1) A yield of 620 mg (MW 367.2, 31%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06824760B2
Source datasetuspto-grants-2004_11
ORD IDord-0db1e37966994f1d89819e901e548e72
Source noteuspto-grants-2004_11