1-Bromo-4-(methylsulphonyl)benzene → HCID 22320754, compound

HRID 1837525Notes

Reaction equation

HRID 1837525 reaction equation
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8](Br)=[CH:7][CH:6]=1)(=[O:4])=[O:3].[CH2:12]([OH:17])[CH2:13][CH2:14][C:15]#[CH:16]>>[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([C:16]#[C:15][CH2:14][CH2:13][CH2:12][OH:17])=[CH:7][CH:6]=1)(=[O:4])=[O:3]

Participants

3

Procedure

Preparation of the title compound with 4-bromophenyl methyl sulphone (5.87 g, 25 mmol) and 4-pentyn-1-ol (2.1 g, 25 mmol) according to the procedure in example 18 yielded 5.12 g (87%) of yellow oil which was characterized as 5-(4-Methanesulfonylphenyl)pent-4-yn-1-ol: NMR (CDCl3) δ 1.88-1.93 (m,2H), 2.56-2.60 (t, J=6.99, 2H), 3.04 (s,3H), 3.80-3.84 (t, J=6.15,2H), 7.56 (d, J=5.1,2H), 7.85(d,J=4.8,2H). MS m/Z 239 (M+H cald. for C12H14O3S 238.3)

Sources & evidence

ORD record
ord-a3f687cffa144680a3b79f01c0a6026a
Source dataset
uspto-grants-2004_08
Patent number
US06784184B2

Reaction notes

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