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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988293Generated: October 31, 2026

Acetaldehyde → N-Et-Tyr(3-tBu)-NHMe

https://huagongshe.com/reaction/1988293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
ReactantTyr(3-tBu)-NHMeHCID 131722741—
SolventWaterHCID 962—
ProductN-Et-Tyr(3-tBu)-NHMeHCID 13172752290%

Reaction Steps

A mixture of Tyr(3-tBu)-NHMe (1.7 g, 6.8 mmol), acetaldehyde (0.76 ml, 13.6 mmol) and dichloromethane (10 ml) was stirred under cooling with ice for 30 min. The reaction mixture was concentrated under reduced pressure under cooling with ice; the thus obtained residue was mixed with methanol (20 ml) and then under cooling with ice with sodium borohydride (0.28 g, 7.4 mmol) and stirred at the same temperature for 15 min. The resultant was mixed with water and extracted with dichloromethane. The organic layer was washed with water, dried and concentrated under reduced pressure under cooling with ice; the thus obtained residue was subjected to silica gel column chromatography (CHCl3:MeOH=20:1), giving N-Et-Tyr(3-tBu)-NHMe (T8) (1.7 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553969B1
Source datasetuspto-grants-2009_06
ORD IDord-f88b4c2680744cbf8fc9fb4ed5fb2d92
Source noteuspto-grants-2009_06