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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253312Generated: October 31, 2026

Carbon Dioxide → HCID 66890939, compound

https://huagongshe.com/reaction/253312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantBoron trifluoride etherateHCID 8000—
ReactantTert-Butyl nitriteHCID 10906—
ReactantHCID 66890928HCID 66890928—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66890939HCID 6689093916.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

A solution of methyl 5-amino-2,3-bis{[2-(methyloxy)ethyl]oxy}benzoate (2.2 g, 7.4 mmol) in 1,2-dimethoxyethane (5 mL) was cooled at −4° C. and then cooled in solid dry-ice. To this mixture was added first boron trifluoride diethyl etherate (1.3 mL, 10 mmol), and then tert-butylnitrite (1.4 mL, 12 mmol), and the resulting mixture was stirred at −4° C. for 2 hours. It was then diluted with ether (100 mL) and a solid precipitated and was collected and washed with ether. The solid was suspended in 1,2,4-trichlorobenzene (20 mL) and heated at 110° C. for 18 hours. After cooling to room temperature, it was applied directly onto a silica gel column with hexane, and then chromatographed (30% ethyl acetate-hexane) to give methyl 5-fluoro-2,3-bis{[2-(methyloxy)ethyl]oxy}benzoate (0.35 g, 1.2 mmol, 16% yield). 1H NMR (400 MHz, CDCl3): 7.05-7.02 (d, d, 1H), 6.83-6.80 (d, d, 1H), 4.20-4.13 (m, 4H), 3.90 (s, 3H), 3.79-3.72 (m, 4H), 3.44 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872014B2
Source datasetuspto-grants-2011_01
ORD IDord-e3da94f08fb54c2781c3c88d00872227
Source noteuspto-grants-2011_01