HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462496Generated: October 30, 2026
Thionyl Chloride → HCID 13457009, compound
https://huagongshe.com/reaction/462496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13457007 | HCID 13457007 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13457009 | HCID 13457009 | 62.9% |
Reaction Steps
A stirred, ice water cooled mixture of 10.25 g (0.0302 mol) of 6,11-dihydro-N-(1-hydroxy-2-methyl-2-propyl)-11-oxodibenz[b,e]oxepin-2-yl acetamide of Example 2, and 100 ml of sieve dried CH2Cl2 was treated dropwise over a few minutes with 3.95 g (0.0332 mol) of thionyl chloride. The solution was then stirred 15 minutes with cooling and overnight (about 16 hours) at ambient temperature. The solution was washed with 10% sodium hydroxide solution, dried (Na2SO4) and concentrated to an oil which was dried by azeotropic distillation of toluene. On standing overnight at 5° C. the oil crystallized. Recrystallization from 12 ml of isopropanol afforded 6.10 g (62.9%) of crystals of 2-(6,11-dihydro-11-oxodibenz[b,e]oxepin-2-yl)methyl-4,4-dimethyloxazoline, m.p. 101°-103.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04515946 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-ba0c9f8d96c640578e9ddf540c61ef5b |
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| Source note | uspto-grants-1985_05 |
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