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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236148Generated: October 31, 2026

Benzenesulfonyl chloride → HCID 46181654, compound

https://huagongshe.com/reaction/2236148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
ReactantBoc-Tyr-OMeHCID 7019130—
SolventTolueneHCID 1140—
ProductHCID 46181654HCID 46181654100%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Boc-L-tyrosine methyl ester 3 (3.0 g, 0.01 mol) and benzenesulfonyl chloride (1.8 g, 0.01 mol) were dissolved in toluene (14.8 g) and then cooled to 0° C. To the mixture was added dropwise triethylamine (1.0 g, 0.01 mol) at 0° C. over 35 min. The mixture was further kept at 0° C. for 3 hrs. The reaction mass was washed with 5% hydrochloric acid (7.3 g) and 5% aqueous sodium bicarbonate (8.4 g) and then concentrated under reduced pressure with a rotary evaporator to give N-Boc-O-benzenesulfonyl-L-tyrosine methyl ester 5 (4.35 g, yield 100%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714157B2
Source datasetuspto-grants-2010_05
ORD IDord-ee79a0d9ff3d41c9b7eb85c9f3f81b22
Source noteuspto-grants-2010_05