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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881746Generated: November 1, 2026

3,3-Dimethyl-1-butyne → HCID 86700848, compound

https://huagongshe.com/reaction/881746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-Dimethyl-1-butyneHCID 13512—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactantp-Chlorophenylboric acidHCID 17810664—
ReactantHCID 86692328HCID 86692328—
CatalystHCID 178418807HCID 178418807—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86700848HCID 8670084876.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A 100 ml heavy wall round bottom flask was charged with the crude intermediate 4-trifluoromethanesulfonyloxy-cyclohex-3-ene-1,1-dicarboxylic acid diethyl ester (4.0 g, 80% purity, 8.55 mmol, 1.0 equiv) from last step, PdCl2(dppf)-CH2Cl2 adduct (0.628 g, 0.769 mmol, 0.09 equiv), 4-chloro-phenylboric acid (2.67 g, 17.1 mmol, 2.0 equiv), tripotassium phosphate (4.54 g, 21.37 mmol, 2.5 equiv), ethanol (8 ml), dimethoxyethane (32.0 ml) and t-butyl acetylene (7.9 g, 97 mmol, 2.0 equiv). The flask was sealed, flushed with nitrogen for three times and stirred at 80° C. for 16 hours. After cooled at room temperature, the reaction mixture was filtered and washed with ethyl acetate (20 ml). The filtrate was concentrated under vacuum and the residue was purified by chromatography (heptanes/ethyl acetate 2/1) to give 4-(4-chloro-phenyl)-cyclohex-3-ene-1,1-dicarboxylic acid diethyl ester (2.2 g, 76%) as colorless oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.27 (t, J=8.00 Hz, 6H) 2.29 (t, J=6.38 Hz, 2H) 2.46 (td, J=6.25, 2.02 Hz, 2H) 2.65-2.85 (m, 2H) 4.21 (q, J=8.00 Hz, 4H) 6.07 (m, 1H) 7.26 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993619B2
Source datasetuspto-grants-2015_03
ORD IDord-03299d46a4994367b580144cf7b2b9c1
Source noteuspto-grants-2015_03