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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492412Generated: October 25, 2026

1-Chloroethyl chloroformate → 7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride

https://huagongshe.com/reaction/492412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactantmethoxy-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 68748342—
Solvent1,2-DichloroethaneHCID 11—
Product7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochlorideHCID 21242906179%

Reaction Steps

The reactions are set up in a 22 L flask, each equipped with a mechanical stirrer, heating mantle, condenser and nitrogen bubbler. Add 1-chloroethyl chloroformate (620 mL, 5.750 mol, 10.0 eq) over 1 hour to methoxy-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine (110 g, 575 mmol, 1.0 eq) dissolved in 1,2-dichloroethane (8.0 L) at 60° C. under nitrogen, in a 22 L flask. The solution turns dark purple over the next 2 hours. Heat the mixture to reflux and stir for 16 hours under nitrogen. The reaction is determined to be complete by TLC. Cool the reaction flask and concentrate under vacuum to an oil. Dissolve the oil in methanol (4 L) and add to a 22 L reaction flask and stir for 16 hours at room temperature under nitrogen. Concentrate the resulting solution under vacuum to an off-white solid 220 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531557B2
Source datasetuspto-grants-2009_05
ORD IDord-41248d370a3846998acd2747a8476014
Source noteuspto-grants-2009_05