1,4-Dioxaspiro[4.5]decan-8-ylmethanol → 9-Benzoyl-3-hydroxymethyl-1,2,3,4-tetrahydrocarbazole
Reaction equation
Cl.[C:2]([N:10]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)N)(=[O:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C1O[C:21]2([CH2:26][CH2:25][CH:24]([CH2:27][OH:28])[CH2:23][CH2:22]2)OC1>C(O)C>[C:2]([N:10]1[C:21]2[CH2:26][CH2:25][CH:24]([CH2:27][OH:28])[CH2:23][C:22]=2[C:17]2[C:12]1=[CH:13][CH:14]=[CH:15][CH:16]=2)(=[O:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-Benzoyl-1-phenylhydrazine hydrochloride (23.8 g.) and 18 g. of 4-hydroxymethylcyclohexanone ethylene ketal in 450 ml. of absolute ethyl alcohol was heated under reflux for four hours. The chilled mixture was filtered, the filtrate was evaporated to dryness under reduced pressure and the resulting residue was dissolved in ether. The ether solution was washed with water, dilute hydrochloric acid, water, dilute sodium bicarbonate, and water, dried and evaporated to dryness to give, after recrystallization from ethyl acetate-hexane, 9.6 g. of 9-benzoyl-3-hydroxymethyl-1,2,3,4-tetrahydrocarbazole; m.p. 105°-107° C.
Workup
- temperatureunder reflux for four hours
- filtrationThe chilled mixture was filtered
- customthe filtrate was evaporated to dryness under reduced pressure
- dissolutionthe resulting residue was dissolved in ether
- washThe ether solution was washed with water, dilute hydrochloric acid, water, dilute sodium bicarbonate, and water
- customdried
- customevaporated to dryness
- customto give
- customafter recrystallization from ethyl acetate-hexane, 9.6 g
Sources & evidence
- ORD record
- ord-ea070daa841b4824ba9bffb6159f76f2
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04028382
Reaction notes
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