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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462496Generated: October 30, 2026

Thionyl Chloride → HCID 13457009, compound

https://huagongshe.com/reaction/462496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 13457007HCID 13457007—
SolventDichloromethaneHCID 6344—
ProductHCID 13457009HCID 1345700962.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515946
Source datasetuspto-grants-1985_05
ORD IDord-ba0c9f8d96c640578e9ddf540c61ef5b
Source noteuspto-grants-1985_05