Sodium Hydroxide → HCID 23667709, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][SH:10])=[CH:5][CH:4]=1.[OH-].[Na+:12]>C(O)C>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][S-:10])=[CH:5][CH:4]=1.[Na+:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(4-methoxyphenyl)methanethiol is stirred in ethanol with sodium hydroxide to form sodium (4-methoxyphenyl)methanethiolate. An equivalent of 1-(chloromethyl)-4-methoxybenzene is added to the mixture, which is stirred overnight. The reaction mixture is then quenched by addition of dilute acid and the product bis(4-methoxybenzyl)sulfide. Subsequently, the bis(4-methoxybenzyl)sulfide is reacted with HBr in acetonitrile to cleave the methoxy protecting groups, followed by neutralization and purification of the bis(4-hydroxybenzyl)sulfide product.
Sources & evidence
- ORD record
- ord-2df8763b9081449fa9ee375eb7e017b9
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07351434B2
Reaction notes
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