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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583241Generated: November 3, 2026

Triethylamine → HCID 11383956, compound

https://huagongshe.com/reaction/1583241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl L-phenylalaninate hydrochlorideHCID 165085—
ReactantN-carbobenzyloxyalanineHCID 736104—
ReactantHCID 7019742HCID 7019742—
SolventDichloromethaneHCID 6344—
ProductHCID 11383956HCID 11383956—

Reaction Steps

Synthesis of p-hydroxybenzoyl-L-alanyl-L-phenylalanine: 0.1 g (0.1 mol) of triethylamine was added to a suspension of 23.0 g (0.1 mol) of L-phenylalanine ethyl ester·HCl in 500 ml of dichloromethane, and to this mixture in an ice bath was added 22.3 g (0.1 mol) of carbobenzoxy-L-alanine, and then 19.2 g (0.1 mol) of 1-ethyl-3(3-dimethyaminopropyl) carbodiimide·HCl was added to the mixture. This mixture was stirred for three hours. This reaction mixture was washed with a 0.1% aqueous solution of Na2CO3 three times and with a 0.1 N HCl solution three times, and then with distilled water three times. Thereafter, the mixture was dried over anhydrous sodium sulfate, and dichloromethane was removed from the mixture under reduced pressure to obtain carbobenzoxy-L-alanyl-L-phenylalanine ethyl ester. This ester was dissolved in 260 ml of 25% HBr in glacial acetic acid, and this solution was stirred for one hour. To this solution was added 5 l of absolute ethyl ether to produce a precipitate. The precipitate was filtered and washed with ethyl ether to obtain L-alanyl-L-phenylalanine ethyl ester·HBr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551272
Source datasetuspto-grants-1985_11
ORD IDord-b71bae26336a4fc1af018dfc7e2df47f
Source noteuspto-grants-1985_11