HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35364Generated: October 30, 2026
Chloroacetyl chloride → HCID 22839463, compound
https://huagongshe.com/reaction/35364
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 13609761 | HCID 13609761 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22839463 | HCID 22839463 | — |
Reaction Steps
A solution of 1.21 g of trans-3,4,4a,5,6,11b-hexahydro-2H-[1]benzoxepino[5,4-b]-1,4-oxazine hydrochloride, prepared according to the procedure of Example 2, and 1.65 ml of triethylamine in 25 ml of methylene chloride is treated dropwise with a solution of 0.70 ml of chloroacetyl chloride dissolved in 10 ml of methylene chloride. The reaction mixture is stirred overnight at room temperature, washed with a dilute solution of hydrochloric acid, followed by a water wash, a wash of dilute sodium hydroxide solution and finally by a wash of a saturated solution of sodium chloride. The reaction mixture is dried over anhydrous magnesium sulfate and evaporated to dryness to obtain 1.44 g of trans-N-chloroacetyl-3,4,4a,5,6,11b-hexahydro-2H-[1]-benzoxepino[5,4-b]-1,4-oxazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766212 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-3c8572f9eb4c498cba0e77d5e3eba59e |
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| Source note | uspto-grants-1988_08 |
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