Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798774Generated: November 1, 2026

4-Methoxybenzyl 2,2,2-Trichloroacetimidate → HCID 57887025, compound

https://huagongshe.com/reaction/1798774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl 2,2,2-TrichloroacetimidateHCID 11087263—
ReactantHCID 57887021HCID 57887021—
CatalystBoron trifluoride etherateHCID 8000—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57887025HCID 5788702534.4%

Reaction Steps

Boron trifluoride etherate (8.0 μL, 65 μmol) was added to a stirred solution of tert-butyl 5-biphenyl-4-yl-2-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-3-hydroxypentanoate (7.88 g, 16.3 mmol) and 4-methoxybenzyl 2,2,2-trichloroethanimidoate (6.88 g, 24.5 mmol) in tetrahydrofuran (40 mL) at 0° C. under nitrogen. The reaction was allowed to warm to room temperature at which stirring was continued for 2 h. A further portion of boron trifluoride etherate (8.0 μL, 65 μmol) was then added and stirring was continued at room temperature for a further 2 h. Two further additions of boron trifluoride etherate (8.0 μL, 65 μmol) followed by stirring at room temperature for 2 h were carried out before evaporation of the solvent. The residue was chromatographed on silica gel (5% to 10% diethyl ether: cyclohexane) to give the title compound (3.39 g, 34%) as a pale yellow oil which was a mixture of diastereomers. LC/MS: 4.81 min; z/e 605, calcd (M+1) 605. 1H NMR (400 MHz: CDCl3): 7.55 (2H), 7.45 (4H), 7.35-6.80 (7H), 4.50 (2H), 3.80 (3H), 3.60 (3H), 2.95 (1H), 2.80 (1H), 2.65 (1H), 1.85 (4H), 1.45 (9H), 0.85 (9H), 0.5 (6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343986B2
Source datasetuspto-grants-2013_01
ORD IDord-1ce7dab77e664f9d828a61e4031ca0f2
Source noteuspto-grants-2013_01