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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847339Generated: October 25, 2026

Water → 1-(5-Tert-Butoxycarbonyl-2-Nitrophenoxy)-2-(5-Methyl-2-Nitrophenoxy)Ethane

https://huagongshe.com/reaction/847339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantBenzene, 2-(2-bromoethoxy)-4-methyl-1-nitro-HCID 13685252—
Product1-(5-Tert-Butoxycarbonyl-2-Nitrophenoxy)-2-(5-Methyl-2-Nitrophenoxy)EthaneHCID 19880870—

Reaction Steps

A mixture of Compound 3e (239 mg, 1 mmol), 1-bromo-2-(5-methyl-2-nitrophenoxy)ethane, see G. Grynkiewicz, et al. (1985), (286 mg, 1.1 mmol), K2CO3 (83 mg, 0.6 mmol) in dry N-methylpyrrolidinone (0.75 mL) was heated at 140° C. for 10 min with protection from moisture, cooled and H2O added dropwise to precipitate the product, Compound 3f. After filtration, recrystallization from EtOH gave a white solid, m.p. 113°-114° C. Yield, 383 mg (92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05141627
Source datasetuspto-grants-1992_08
ORD IDord-643677538a22494e9ce56617fc2e9b36
Source noteuspto-grants-1992_08