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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745927Generated: November 1, 2026

Imidazole → HCID 69965447, compound

https://huagongshe.com/reaction/1745927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
ReactantHCID 69599737HCID 69599737—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 69965447HCID 6996544780.2%

Reaction Steps

A mixture of p-methylphenyl 2-deoxy-2-phthalimido-3-O-benzoyl-1-thio-β-D-glucopyranoside (70.0 mg, 0.1349 mmol), tert-butylchlorodiphenylsilane (83.2 mg, 0.2968 mmol), and imidazole (27.8 mg, 0.4047 mmol) in DMF (4 mL) was stirred for 4 h. The mixture was diluted with EtOAc (35 mL) and washed with water (3×10 mL). The organic layer was dried over Na2SO4 and concentrated. The residue was purified by column chromatography on silica gel (hexanes/EtOAc 4:1 to 3:1) to give product (82.0 mg, 80%) as a thick oil: 1H NMR (500 MHz, CDCl3) δ 7.85 (dd, J=83, 1.1 Hz, 2H), 7.80 (d, J=6.4 Hz, 1H), 7.73–7.77 (m, 5H), 7.60–7.66 (m, 2H), 7.28–7.47 (m, 11H), 7.00 (d, J=8.1 Hz, 2H), 5.93 (dd, J=10.3, 8.9 Hz, 1H), 5.77 (d, J=10.4 Hz, 1H), 4.47 (t, J=10.3 Hz, 1H), 4.01–4.09 (m, 2H), 3.97 (t, J=9.3 Hz, 1H), 3.78 (dt, J=9.6, 4.3 Hz, 1H), 3.18 (br. s, 1H), 2.28 (s, 3H), 1.09 (s, 9H); 13C NMR (125 MHz, CDCl3) δ 167.88, 167.17, 166.84, 138.14, 135.65, 135.60, 134.17, 134.04, 133.30, 133.26, 132.95, 132.91, 131.55, 131.21, 129.84, 129.77, 129.61, 128.90, 128.30, 127.79, 127.76, 123.54, 123.50, 83.29, 79.76, 75.38, 71.05, 64.12, 53.54, 26.80, 21.10, 19.22; HRMS (M+Na) calcd for C44H43O7NSSiNa 780.2427, found 780.2460 washed with H2O (15 mL), sat. NaHCO3 (15 mL), and brine (10 mL). The organic layer was dried (Na2SO4) and concentrated. The residue was subjected to column chromatography (hexanes/EtOAc 3:1) to give product (280 mg, 96%) as a foam: 1H NMR (500 MHz, CDCl3) δ 7.86 (dd, J=8.4, 1.0 Hz, 2H), 7.82 (d, J=6.4 Hz, 1H), 7.75 (d, J=6.3 Hz, 1H), 7.65–7.69 (m, 2H), 7.48 (t, J=75 Hz, 1H), 7.28–7.37 (m, 9H), 7.03 (d, J=7.7 Hz, 2H), 5.90 (dd, J=10.2, 8.8 Hz, 1H), 5.73 (d, J=10.4 Hz, 1H), 4.58–4.65 (ABq, J=11.9 Hz, 2H), 4.48 (t, J=10.4 Hz, 1H), 3.81–3.95 (m, 4H), 3.15 (d, J=3.7 Hz, 1H), 2.29 (s, 3H); 13C NMR (125 MHz, CDCl3) δ 167.86, 167.20, 166.86, 138.38, 137.86, 134.22, 134.11, 133.49, 133.38, 131.59, 131.27, 129.88, 129.66, 128.90, 128.43, 128.37, 127.77, 127.72, 123.58, 83.47, 78.71, 75.27, 73.72, 71.41, 70.10, 53.54, 21.14; HRMS (M+Na) calcd for C35H31O7NSNa 632.1719. found 632.1747.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019131B2
Source datasetuspto-grants-2006_03
ORD IDord-07f524f138b843a0b50d573163897b48
Source noteuspto-grants-2006_03