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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506679Generated: October 31, 2026

Oxalyl chloride → HCID 86762562, compound

https://huagongshe.com/reaction/1506679

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 numberUS09220795B2
Source datasetuspto-grants-2015_12
ORD IDord-5b1d959ff351463b83378a98f41a6bd6
Source noteuspto-grants-2015_12