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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236149Generated: October 30, 2026

Triethylamine → HCID 46181731, compound

https://huagongshe.com/reaction/2236149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBoc-Tyr-OMeHCID 7019130—
SolventTolueneHCID 1140—
ProductHCID 46181731HCID 4618173196.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Boc-L-tyrosine methyl ester 3 (29.5 g, 0.1 mol) and triethylamine (20.2 g, 0.2 mol) were dissolved in toluene (147.7 g) and then cooled to 0° C. To the mixture was added dropwise methanesulfonyl chloride (13.8 g, 0.12 mol) at 0° C. over 40 min. The mixture was further kept at 0° C. for 25 min. The reaction mass was washed with 5% hydrochloric acid (72.9 g) and 5% aqueous sodium bicarbonate (84.0 g), dried over magnesium sulfate, and then concentrated under reduced pressure with a rotary evaporator. After crystallization from the concentrate mass with n-hexane, precipitated crystals were collected by filtration and dried to give N-Boc-O-methanesulfonyl-L-tyrosine methyl ester 6 (36.0 g, yield 96%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714157B2
Source datasetuspto-grants-2010_05
ORD IDord-1ff0abb47e054f4ea4ed00461e56bb04
Source noteuspto-grants-2010_05