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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485358Generated: October 31, 2026

Methyl iodide → HCID 178503520, compound

https://huagongshe.com/reaction/1485358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantThioureaHCID 2723790—
ReactantSodium ethoxideHCID 2723922—
Reactant1-tert-Butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylateHCID 4436570—
SolventEthanolHCID 702—
ProductHCID 178503520HCID 17850352073%

Reaction Steps

To solution of 5-oxo-azepane-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester (10.5 g, 0.04 mol) in EtOH (168 mL) was added NaOEt (8.1 g, 0.12 mol) and thiourea (4.2 g, 0.06 mol). The mixture was heated at reflux for 12 h. The mixture was cooled, treated with MeI (3.0 mL, 0.05 mol) drop-wise, and stirred at rt for 1 h. The mixture was concentrated and the residue was dissolved in water and acidified to pH=7 with HOAc (a precipitate formed). The solid was filtered to give the title compound (8.4 g, 73%), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422293B2
Source datasetuspto-grants-2016_08
ORD IDord-5fa32e53426740d694b2788ca6c44718
Source noteuspto-grants-2016_08