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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703001Generated: November 3, 2026

Sodium hydride → HCID 20524441, compound

https://huagongshe.com/reaction/1703001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 20524446HCID 20524446—
ReactantHCID 178514229HCID 178514229—
SolventAcetonitrileHCID 6342—
ProductHCID 20524441HCID 20524441—

Reaction Steps

1.0 g of 50% sodium hydride dispersion in mineral oil was added at room temperature to a solution of 4.0 g of 2-bromobenzoyl amide in 25 ml of dry acetonitrile. After stirring for approximately 30 minutes at room temperature, 4.78 g of 4-(1-phenylethoxy)phenylisocyanate were added, the reaction mixture becoming warm and substantially homogeneous. After stirring for another approximately 16 hours at room temperature the reaction mixture was filtered. The filtrate was acidified with dilute hydrochloric acid. The resulting precipitate was sucked off and washed successively with acetonitrile, ethanol and petroleum ether (40-60). The desired product was obtained in a yield of 1.85 g; the melting point was determined on a "Kofler bank" and was 155.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04350706
Source datasetuspto-grants-1982_09
ORD IDord-29057b0030734d63b126458aae0b1065
Source noteuspto-grants-1982_09