Hydrochloric Acid → HCID 67809084, compound
Reaction equation
[Cl:1][C@H:2]1[C@@H:10]2[C@@H:6]([CH2:7][N:8](C(Cl)=O)[CH2:9]2)[C:5]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:4][CH2:3]1.Cl>O1CCCC1>[ClH:1].[Cl:1][C@H:2]1[C@@H:10]2[C@@H:6]([CH2:7][NH:8][CH2:9]2)[C:5]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH2:4][CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 0.4 g of (3aR,7R,7aR)-7-chloro-2-chlorocarbonyl-4,4-diphenylperhydroisoindole in 6 cm3 of a 1N aqueous solution of hydrochloric acid and 14 cm3 of tetrahydrofuran is heated at 80° C. for 9 hours, with stirring. The reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa). 0.35 g of (3aR,7R,7aR)-7-chloro-4,4-diphenylperhydroisoindole hydrochloride is obtained in the form of a white solid.
Workup
- concentrationThe reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa)
Sources & evidence
- ORD record
- ord-5f1052a761fb414d83a00b319c39bbd3
- Source dataset
- uspto-grants-1995_09
- Patent number
- US05451601
Reaction notes
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