HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130803Generated: October 25, 2026
1-Chloroethyl chloroformate → 7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride
https://huagongshe.com/reaction/130803
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | methoxy-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine | HCID 68748342 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride | HCID 21242906 | 179% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381719B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-e6112d2fb9234db7b92b5785d797fa33 |
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| Source note | uspto-grants-2008_06 |
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