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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629586Generated: October 31, 2026

Oxalyl chloride → HCID 86762562, compound

https://huagongshe.com/reaction/1629586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 66679764HCID 66679764—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 86762562HCID 86762562—

Reaction Conditions

Temperature20 °C

Reaction Steps

9-(2-Benzyloxy-ethyl)-8-chloro-5-methoxy-2,3,4,9-tetrahydro-1H-carbazole-4-carboxylic acid (7) (1.5 g, 3.7 mmol) was dissolved in dichloromethane (50 mL) and oxalyl chloride (700 mg, 5.5 mmol, 470 μL) and DMF (1 drop) were added and the reaction stirred at 20° C. for 2 h. There was a moderate evolution of gas for about 30 min as the reaction proceeded. The reaction was then concentrated in vacuo to give 9-(2-Benzyloxy-ethyl)-8-chloro-5-methoxy-2,3,4,9-tetrahydro-1H-carbazole-4-carbonyl chloride (8) as a gum which was used into the next step without purification. The structure was confirmed by 13C NMR (75 MHz; CDCl3): δC 20.8, 22.1, 26.4, 44.2, 51.8, 55.1, 70.7, 73.3, 100.7, 106.0, 108.6, 119.5, 123.4, 127.3, 127.7, 128.3, 131.9, 138.0, 138.2, 152.0. and 176.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08790619B2
Source datasetuspto-grants-2014_07
ORD IDord-90461c70c82d4824ba8188098284b946
Source noteuspto-grants-2014_07