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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154862Generated: November 1, 2026

Oxalyl chloride → HCID 12905148, compound

https://huagongshe.com/reaction/1154862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 12336141HCID 12336141—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 12905148HCID 12905148—

Reaction Steps

Oxalyl chloride (5.3 g) was added to a solution of 2,3-diacetoxybenzamide (4.0 g) in 1,2-dichloroethane (40 ml) while stirring under cooling. The mixture was gradually heated to a reflux temperature and allowed to react under reflux for 10 hours. Then, the solvent and excess oxalyl chloride were distilled off under reduced pressure to give 2,3-diacetoxybenzoyl isocyanate, which was dissolved in dried dichloromethane (40 ml) for the subsequent reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04298605
Source datasetuspto-grants-1981_11
ORD IDord-964839d61d834f1a80f09a12e063dfe8
Source noteuspto-grants-1981_11