Carbon tetrabromide → HCID 79997855, compound
Reaction equation
[Br:1][C:2]1[S:6][C:5]([CH2:7]O)=[CH:4][C:3]=1[CH3:9].C(Br)(Br)(Br)[Br:11].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O1CCCC1>[Br:1][C:2]1[S:6][C:5]([CH2:7][Br:11])=[CH:4][C:3]=1[CH3:9]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a tetrahydrofuran solution (1.0 mL) of (5-bromo-4-methylthiophen-2-yl)methanol (33.7 mg, 0.163 mmol) synthesized in Reference Synthesis Example 100, carbon tetrabromide (59.4 mg, 0.179 mmol) and triphenylphosphine (47.0 mg, 0.179 mmol) were added and the resultant solution was stirred at room temperature for 20 hours. After completion of the reaction, the reaction solution was filtered and the obtained filtrate was concentrated under reduced pressure to obtain the title compound as a crude product.
Workup
- additionwere added
- customAfter completion of the reaction
- filtrationthe reaction solution was filtered
- concentrationthe obtained filtrate was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-b1fc181e846e4139b63826a7187dd7d0
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09403798B2
Reaction notes
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