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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593638Generated: October 31, 2026

Ammonium Hydroxide → HCID 69235318, compound

https://huagongshe.com/reaction/1593638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 13491214HCID 13491214—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 69235318HCID 69235318—

Reaction Conditions

Temperature0 °C

Reaction Steps

2,3,4,9-tetrahydro-1H-carbazole-3-carboxylic acid (30.4 g, 141 mmol), was suspended in 450 ml of methylene chloride and cooled to 0° C. Oxalyl chloride (14.8 mL, 169 mmol) was added dropwise, followed by two drops of DMF. The resulting mixture was allowed to warm to room temperature and was stirred for 24 h. After re-cooling to 0° C., 450 mL of conc. aqueous ammonium hydroxide were added dropwise. The yellow precipitate that formed was collected by vacuum filtration. After drying, the title compound weighed 17.4 g (58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297704B2
Source datasetuspto-grants-2007_11
ORD IDord-c2929f08d2ec4724ad6b823a1b5a92f6
Source noteuspto-grants-2007_11