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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392832Generated: October 29, 2026

Trichloroacetyl chloride → HCID 67618536, compound

https://huagongshe.com/reaction/2392832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
Reactant(βR)-β-Amino-α,α-dimethylbenzeneethanolHCID 11240681—
SolventPyridineHCID 1049—
ProductHCID 67618536HCID 6761853667%

Reaction Steps

To a solution of (13) (1.413 g, 8.56 mmol) in pyridine (24 ml) at 0° C. was added trichloroacetyl chloride (1.05 ml, 9.41 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 (14) (1.782 g, 65%) as a solid which was recrystallised from ether/40-60 petroleum ether; mp 97° C.; νmax (CHCl3) 1716 cm-1 ; [α]D24 (c 1 in CHCl3)=-55.5; (Found: C, 46.41; H, 4.26; N, 4.49. C12H14Cl3NO2 requires C, 46.40; H, 4.54; N, 4.51%); δH (200 MHz; CDCl3) 1.06 (3H, s, C(CH3)2), 1.39 (3H, s, C(CH3)2), 1.94 (1H, s, OH), 4.70 (1H, d, J=8.5, CHCH), 7.29-7.39 (5H, m, ArCH); δC (125 MHz; CDCl3) 27.70 (CH3), 27.86 (CH3), 63.06 (CH), 75.52 (C), 92.97 (CCl3), 128.13 (ArCH), 128.35 (ArCH), 128.71 (ArCH), 137.88 (C), 161.51 (CO); m/z (CI-, NH3) 310 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05801249
Source datasetuspto-grants-1998_09
ORD IDord-a7b428eb9e9a43fe8f5a5756a95d8622
Source noteuspto-grants-1998_09