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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585976Generated: October 31, 2026

Acetic Anhydride → HCID 53976707, compound

https://huagongshe.com/reaction/1585976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 53676929HCID 53676929—
ProductHCID 53976707HCID 53976707—

Reaction Steps

4.0 g (12.5 mmoles) of 1-(4-aminostyryl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine (the compound of Example 68) are suspended in 20 ml of acetic anhydride. The suspension is stirred at room temperature for 1 hour. In the meantime the starting substance gets dissolved, the desired product begins to separate and the reaction mixture becomes thick. The separated product is filtered, washed three times with 25 ml each of diethyl ether and dried at a temperature between 80° C. and 100° C. Thus 4.0 g of the desired product are obtained. In order to purify the crude product it is boiled in 15 ml of 50% ethanol for 15 minutes, cooled, filtered, washed three times with 5 ml each of 50% ethanol and dried at a temperature between 80° C. and 100° C. Thus 3.87 g (85.6%) of the desired product are obtained. M.p.: 218-220° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05942506
Source datasetuspto-grants-1999_08
ORD IDord-eafc2cd97b13448caee0b55412e52567
Source noteuspto-grants-1999_08