Triethylamine → 4-Benzyl-2-(2-chloroethyl)-2,3-dihydro-1,4-benzoxazepin-5(4H)-one
Reaction equation
[CH2:1]([N:8]1[CH2:12][CH2:11][CH:10]([O:13][C:14]2[CH:22]=[CH:21][CH:20]=[CH:19][C:15]=2[C:16](O)=[O:17])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.S(Cl)([Cl:32])=O>>[CH2:1]([N:8]1[C:16](=[O:17])[C:15]2[CH:19]=[CH:20][CH:21]=[CH:22][C:14]=2[O:13][CH:10]([CH2:11][CH2:12][Cl:32])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
Procedure
To 85.7 g (0.29 mole) of 2-[(1-benzyl-3-pyrrolidinyl)oxy]-benzoic acid was added 150 ml of thionyl chloride. The solution stood for 15 min and was then refluxed 30 min. and concentrated in vacuo. The residue was twice treated with 250 ml of chloroform and concentrated in vacuo. The residue was dissolved in 500 ml of chloroform and 101 g (1 mole) of triethylamine added slowly with stirring. The solution was refluxed 1 hr. and concentrated in vacuo. The residue was partitioned between 50% ethyl acetate-50% isopropyl ether and dilute hydrochloric acid. The organic layer was washed with dilute sodium hydroxide and concentrated. The residue was crystallized 5 times from isopropyl ether-ethyl acetate. Yield of product was 23.8 g (26%), m.p. 145.0°-147° C.
Workup
- temperaturewas then refluxed 30 min.
- concentrationconcentrated in vacuo
- additionThe residue was twice treated with 250 ml of chloroform
- concentrationconcentrated in vacuo
- dissolutionThe residue was dissolved in 500 ml of chloroform
- temperatureThe solution was refluxed 1 hr
- concentrationand concentrated in vacuo
- customThe residue was partitioned between 50% ethyl acetate-50% isopropyl ether and dilute hydrochloric acid
- washThe organic layer was washed with dilute sodium hydroxide
- concentrationconcentrated
- customThe residue was crystallized 5 times from isopropyl ether-ethyl acetate
Sources & evidence
- ORD record
- ord-7e2a259ab7b140b38fa5086a1b44bdb6
- Source dataset
- uspto-grants-1987_02
- Patent number
- US04642343
Reaction notes
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