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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392827Generated: October 30, 2026

Trichloroacetyl chloride → HCID 67617846, compound

https://huagongshe.com/reaction/2392827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantHCID 12192619HCID 12192619—
SolventPyridineHCID 1049—
ProductHCID 67617846HCID 6761784688%

Reaction Steps

To a solution of (8) (2.573 g, 14.37 mmol) in pyridine (50 ml) at 0° C. was added trichloroacetyl chloride (1.93 ml, 17.25 mmol). After stirring at this temperature for 10 minutes, the reaction mixture was stirred overnight at room temperature. The reaction was quenched by the addition of saturated aqueous sodium chloride solution, after which the product was extracted with dichloromethane and the combined organic extracts were washed with hydrochloric acid (1M). Concentration in vacuo and purification by flash column chromatography using 30% ethyl acetate/40-60 petroleum ether as eluant furnished the title compound (9) (4.093 g, 88%) as a solid; mp 88° C.; νmax (CDCl3) 1713 cm-1 ; [α]D24 (c 0.8 in CHCl3)=-26.8; (Found: C, 48.32; H, 4.61; N, 4.13. C13H16Cl3NO2 requires C, 48.16; H, 4.97; N, 4.32%); δH (300 MHz; CDCl3) 1.32 (3H, S, C(CH3)2), 1.40 (3H, s, C(CH3)2), 1.91 (1H, s, OH), 2.75 (1H, dd, J=10.9 and 14.2, CH2Ph), 3.20 (1H, dd, J=4.04 and 14.2, CH2Ph), 4.04-4.13 (1H, m, CHCH2), 6.80 (1H, d, J=9.3, NH); δC (125 MHz; CDCl3) 27.18 (CH3), 27.74 (CH3), 35.43 (CH2), 60.25 (CH), 72.92 (C), 93.00 (CC13), 126.89 (CH), 128.78 (CH), 129.33 (CH), 137.66 (C), 162.07 (CO); m/z (CI+, NH3) 324 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05801249
Source datasetuspto-grants-1998_09
ORD IDord-59186f6b55a342cf978883f68f7eebbd
Source noteuspto-grants-1998_09