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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67238Generated: October 26, 2026

Hydrochloric Acid → HCID 20528325, compound

https://huagongshe.com/reaction/67238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoinHCID 8400—
ReactantVeratraldehydeHCID 8419—
ReactantPotassium CyanideHCID 9032—
Reactanto-FluorobenzaldehydeHCID 67970—
Reactant1,3-Diazepane-2-thioneHCID 736589—
Reactant3,4-Dimethoxy-2'-fluorobenzoinHCID 20528310—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
ProductHCID 20528325HCID 20528325—

Reaction Steps

A mixture consisting of 16.6 g. of veratraldehyde, 12.5 g. of o-fluorobenzaldehyde, 8 g. of potassium cyanide, and 100 ml of 65% ethanol is reacted as described in Example 20, yielding 12.5 g. of 3,4-dimethoxy-2'-fluorobenzoin, m.p. 126°-128° C. A 5.8 g. portion of the benzoin derivative is converted to its methanesulfonate ester by the procedure of Example 20, giving 6.7 g. of the ester melting at 111°-113° C. 2.58 g. of the methanesulfonate ester, 0.91 g. of hexahydro-2H-1,3-diazepin-2-thione, and 55 ml. of acetone are mixed and left at room temperature for three days. 7 ml. of 2 N ethanolic hydrogen chloride are added, yielding 2.2 g. of the title compound, melting at 192°-194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04344954
Source datasetuspto-grants-1982_08
ORD IDord-2c17cee5591046558cc1b46ca1a3b269
Source noteuspto-grants-1982_08