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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600150Generated: October 30, 2026

Trichloroacetonitrile → HCID 131728731, compound

https://huagongshe.com/reaction/600150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetonitrileHCID 11011—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium cerium-nitrateHCID 57418452—
ReactantHCID 86631772HCID 86631772—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 131728731HCID 13172873194%

Reaction Steps

4-Methoxyphenyl 2-O-acetyl-4-O-benzyl-α-L-rhamnopyranoside (12) (4.57 g, 11.36 mmol) was dissolved in 60 mL of pyridine. FmocCl (5.88 g, 22.73 mmol) was added in one portion and the mixture stirred for 2 h at room temperature. Pyridine was removed in vacuo and the residue adsorbed on silica gel. 6.21 g (88%) of pure 4-methoxyphenyl 2-O-acetyl-4-O-benzyl-3-O-fluorenylmethoxycarbonyl-α-L-rhamnopyranoside were obtained by column chromatography (5:1→4:1→3:1 hexane/EtOAc). 4-Methoxyphenyl 2-O-acetyl-4-O-benzyl-3-O-fluorenylmethoxycarbonyl-α-L-rhamnopyranoside (3.10 g, 4.96 mmol) was dissolved in a mixture of 55 mL of toluene, 80 mL of acetonitrile and 55 mL of water. Cerium ammonium nitrate (21.7 g, 39.7 mmol) was added and the mixture was vigorously stirred for 80 min at room temperature. After TLC showed complete removal of the MP group, the phases of the mixture were separated, the organic phase was washed 2 times with water, saturated aqueous NaHCO3, then again once with water, dried over Na2SO4 and was concentrated. The resulting crude product was adsorbed on silica gel and purified by column chromatography (3:1→2:1 hexane/EtOAc) to afford 1.95 g (76%) of 2-acetyl-4-benzyl-3-fluorenylmethoxycarbonyl-L-rhamnopyranoside as a slightly yellow solid. This compound (675 mg, 1.30 mmol) was dissolved in 6 mL of tricloroacetonitrile and 7 mL of dichloromethane. A catalytic amount of sodium hydride (10 mg) was added and the mixture stirred for 60 min. The solvent was removed in vacuo and the residue purified by flash column chromatography (2:1 hexane/EtOAc) to afford 810 mg (94%) of 13 (only traces of P product) as a slightly yellow oil: [α]D: −17.3 (c=0.51, CHCl3), IR (thin film, CHCl3): 3026, 1754, 1672, 1451, 1380, 1262, 1067 cm−1. 1H NMR (CDCl3, 300 MHz) δ 1.41 (d, J=6.0 Hz, 3H), 2.22 (s, 3H), 3.69 (t, J=9.3 Hz, 1H), 4.11 (m, 1H), 4.33 (m, 2H), 4.52 (m, 1H), 4.68 (d, J=11.1 Hz, 1H), 4.86 (d, J=11.1 Hz, 1H), 5.26 (dd, J=12.3 Hz, J=3.3 Hz, 1H), 5.61 (m, 1H), 6.23 (s, 1H), 7.28 (m, 7H), 7.39 (m, 2H), 7.60 (m, 2H), 7.77 (d, J=6.6 Hz, 2H), 8.71 (s, 1H). 13C NMR (CDCl3, 75 MHz) 18.1, 21.0, 46.7, 68.4, 70.3, 70.6, 75.5, 75.6, 77.8, 94.7, 120.0, 124.9, 125.1, 127.1, 127.7, 127.8, 127.9, 128.4, 137.4, 141.1, 141.2, 142.9, 143.4, 154.0, 160.0, 169.6. MALDI-HRMS: m/z [M+Na]+ calcd 684.0929, obsd 684.0939.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07901687B2
Source datasetuspto-grants-2011_03
ORD IDord-e8c7e70b2d0145688d74260e4eb6cfae
Source noteuspto-grants-2011_03