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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704665Generated: October 29, 2026

Phenylacetyl chloride → HCID 14348999, compound

https://huagongshe.com/reaction/704665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
ReactantHCID 14348987HCID 14348987—
SolventChloroformHCID 6212—
ProductHCID 14348999HCID 14348999—

Reaction Steps

To a cooled solution of 2,3,4,5-tetrahydro-1-(p-trifluoromethylphenoxy)-3-benzazepine of Example 1 (5.8 g. 0.019 mole) and triethylamine (2.3 g, 0.023 mole) in chloroform (75 ml) was slowly dropped phenylacetyl chloride (3.5 g. 0.023 mole) in chloroform (10 ml). After stirring at ambient temperature overnight the reaction mixture was concentrated to an oil. The oil was dissolved in ether, then washed with water, dilute HCl (10%), again with water and dried (saturated NaCl, anhydrous (MgSO4). The solution was filtered, concentrated to an oil which was extracted with boiling hexanes and then concentrated to an oil (6.8 g, 84%). A sample was distilled to yield an oil of 3-phenylacetyl-2,3,4,5-tetrahydro-1-(p-trifluoromethylphenoxy)-3-benzazepine, 240°-250° C./0.1 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988690
Source datasetuspto-grants-1991_01
ORD IDord-12a1e649b1ab43ef932b341b3528c6d8
Source noteuspto-grants-1991_01