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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018286Generated: October 31, 2026

1,2-Dichloroethane → HCID 86585259, compound

https://huagongshe.com/reaction/1018286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAmmoniaHCID 222—
ReactantCitric AcidHCID 311—
ReactantAcetic AnhydrideHCID 7918—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-(tert-Butoxycarbonyl)-3-iodo-L-tyrosineHCID 15545208—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventIsopropanolHCID 3776—
ProductHCID 86585259HCID 86585259—

Reaction Steps

To a solution of N-Boc-3-iodotyrosine (0.380 g, 0.93 mmol) in pyridine (1 mL) were added acetic anhydride (105 μL, 1.1 mmol) and DMAP (10 mg, cat). The solution was stirred 1.5 h then diluted in 5% citric acid (20 mL), and the product extracted with EtOAc. The organic solution was evaporated and the residue dissolved in MeCN (4 mL). To the stirred cold (ice bath) solution were added EDC (0.196 g, 1.0 mmol) and HOBt (0.135 g, 1.0 mmol). After stirring for 1 h, a 2 N solution of ammonia in iPrOH (3 mL) was added. The suspension was stirred 1 h at 5° C., the solid was filtered, the filtrate evaporated and the residue purified by flash chromatography (gradient 3-5% MeOH/chloroform) to yield N-Boc-O-acety-3-iodotyrosine amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479508B1
Source datasetuspto-grants-2002_11
ORD IDord-50bac30a98c64f61a0a82db87e51a682
Source noteuspto-grants-2002_11