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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzyl 2,2,2-Trichloroacetimidate | HCID 11087263 | — |
| Reactant | HCID 57887021 | HCID 57887021 | — |
| Catalyst | Boron trifluoride etherate | HCID 8000 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57887025 | HCID 57887025 | 34.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343986B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-1ce7dab77e664f9d828a61e4031ca0f2 |
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| Source note | uspto-grants-2013_01 |
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