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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007723Generated: October 30, 2026

1,2-Dichloroethane → HCID 86585259, compound

https://huagongshe.com/reaction/1007723

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 numberUS06794404B2
Source datasetuspto-grants-2004_09
ORD IDord-0227350579d345fb90220001abbee975
Source noteuspto-grants-2004_09