HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380861Generated: October 26, 2026
Ethyl Acetate → 1-(7-Methoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl)-3-chloropropane
https://huagongshe.com/reaction/1380861
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Chloro-3-iodopropane | HCID 81363 | — |
| Reactant | 7-Methoxy-4,5-dihydro-1H-benzo[D]azepin-2(3H)-one | HCID 13520689 | — |
| Solvent | Tetramethylurea | HCID 12437 | — |
| Product | 1-(7-Methoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl)-3-chloropropane | HCID 13520690 | — |
Reaction Steps
First, 7-methoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one (1.15 g, 6 mmol) is dissolved in absolute tetramethylurea (30 ml), mixed with 55% sodium hydride dispersion in oil (300 mg) and stirred for 2 hours at 20°-25° C. under a nitrogen atmosphere. The resulting reaction mixture is added dropwise, with stirring, at 15°-20° C. under a nitrogen atmosphere to 1-chloro-3-iodopropane (1.6 g, 7.8 mmol) dissolved in tetramethylurea (20 ml) and stirred for 3 hours at ambient temperature. Then, ethyl acetate (300 ml) are added and the mixture is extracted six times with water. The organic solution is dried over magnesium sulphate, concentrated by evaporation and the residue is purified oer a silica gel column with methylene chloride and increasing amounts of ethanol (up to 2%). Yield: 410 mg. IR spectrum (methylene chloride): 1650 cm-1 (C=O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04584293 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-fce52bc5e8ee4708b9ae8212cf56dbf0 |
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| Source note | uspto-grants-1986_04 |
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