Chloroacetyl chloride → HCID 737111, compound
Reaction equation
[Cl:1][CH2:2][C:3](Cl)=[O:4].[C:6]12([OH:16])[CH2:15][CH:10]3[CH2:11][CH:12]([CH2:14][CH:8]([CH2:9]3)[CH2:7]1)[CH2:13]2>C(Cl)(Cl)Cl>[Cl:1][CH2:2][C:3]([O:16][C:6]12[CH2:13][CH:12]3[CH2:11][CH:10]([CH2:9][CH:8]([CH2:14]3)[CH2:7]1)[CH2:15]2)=[O:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
There was added slowly at 10° C. and under nitrogen 24 ml of chloracetyl chloride to 30.5 g (0.2 mole) of 1-adamantanol and 12 g of magnesia in suspension in 400 ml of chloroform; it was then brought under reflux for some hours. It was cooled, the inorganic material was filtered off and the solvent evaporated. The crude product was crystallized in hexane. 90% of the product melting 79° C. (capillary) was obtained.
Workup
- temperatureunder reflux for some hours
- temperatureIt was cooled
- filtrationthe inorganic material was filtered off
- customthe solvent evaporated
- customThe crude product was crystallized in hexane
- custommelting 79° C.
- customwas obtained
Sources & evidence
- ORD record
- ord-2687085fa81f4aad87c3853eb63050cc
- Source dataset
- uspto-grants-1984_06
- Patent number
- US04456611
Reaction notes
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