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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213173Generated: November 1, 2026

Hydrochloric Acid → Cga-380778

https://huagongshe.com/reaction/2213173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
ReactantFormamide, N-[2-[3-methoxy-4-(2-propynyloxy)phenyl]ethyl]-HCID 11379286—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
ProductCga-380778HCID 11474256—

Reaction Conditions

Temperature-78 °C

Reaction Steps

N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-formamide (34 g, 0.14 mol) and triethylamine (34 g, 0.34 mol) are dissolved in dichloromethane (120 ml). Bis(trichloromethyl) carbonate (triphosgene, 16 g, 55 mmol) in dichloromethane (80 ml) is added at +5° C. The mixture is stirred for 4 hours at +5° C. and then cooled to −78° C. A solution of titanium tetrachloride (28 g, 0.15 mol) in dichloromethane (150 ml) is added and the mixture is stirred for 2 hours at −40° C. 4-Chlorobenzaldehyde (20 g, 0.14 mol) in dichloromethane (70 ml) is added dropwise and the mixture is stirred for 17 hours at room temperature. The mixture is hydrolyzed with 5N HCl (80 ml), stirred 30 minutes at room temperature and washed with water. After evaporation of the organic layer the residue is submitted to flash-chromatography (ethyl acetate/hexane) to give 2-(4-chloro-phenyl)-2-hydroxy-N-[2-(3-methoxy-4-prop-2-ynyloxy -phenyl)-ethyl]-acetamide. 1H-NMR (300 MHz, CDCl3, δ(ppm)): 2.54 (t, 1H, CO≡CH), 2.72 (t, 2H, CH2CH2), 3.53 (t, 2H, CH2CH2), 3.84 (s, 3H, OCH3), 4.78 (m, 2H, OCH2), 4.98 (s, 1H, CHOH), 6.07 (bs, 1H, NH), 6.53–7.38 (m, 7H, CH arom.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105545B2
Source datasetuspto-grants-2006_09
ORD IDord-858d388b694f485693a22a39583abe26
Source noteuspto-grants-2006_09