Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424983Generated: November 2, 2026

Tert-Butyl nitrite → HCID 68405889, compound

https://huagongshe.com/reaction/1424983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 68406358HCID 68406358—
CatalystCupric ChlorideHCID 24014—
SolventMethanolHCID 887—
ProductHCID 68405889HCID 68405889—

Reaction Conditions

Temperature50 °C

Reaction Steps

Ethyl 2-[bis(tert-butoxycarbonyl)amino]-4-propanoyl-1,3-thiazole-5-carboxylate obtained in Example (62f) (270.5 mg, 0.63 mmol) was dissolved in methanol (2 mL). A 4 N hydrochloric acid/ethyl acetate solution (6 mL) was added, and the mixture was stirred at 50° C. for 50 minutes. The reaction solution was washed with saturated aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The same operation as in Example (22c) was performed using the resulting crude product, copper chloride (96 mg, 0.71 mmol) and tert-butyl nitrite (86 μL, 0.72 mmol), to obtain 49.0 mg of the title compound as a colorless oily substance (31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-47396a2266e5403ebf9b71de2e9f1a1b
Source noteuspto-grants-2015_01