4-Hydroxybenzaldehyde → 4-Formylphenyl methanesulfonate
Reaction equation
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[OH:6][C:7]1[CH:14]=[CH:13][C:10]([CH:11]=[O:12])=[CH:9][CH:8]=1.N1C=CC=CC=1>>[CH:11]([C:10]1[CH:13]=[CH:14][C:7]([O:6][S:2]([CH3:1])(=[O:4])=[O:3])=[CH:8][CH:9]=1)=[O:12]Participants
4
Conditions
- Temperature
- 0 °C
Procedure
At 0° C., methanesulfonyl chloride (9.51 ml, 0.123 mol) was added to a solution of 4-hydroxybenzaldehyde (15 g, 0.123 mol) in pyridine (12.91 ml, 0.160 mol). The reaction mixture was stirred at 0° C. for 3 h and left at room temperature for 16 h. It was given onto conc. hydrochloric acid/ice (200 ml/200 ml). The mixture was extracted with ethyl acetate (4×300 ml). The combined organic layers were washed with a 5% aqueous solution of sodium hydrogen carbonate (3×200 ml) and brine (100 ml). They were dried over magnesium sulphate. The solvent was removed in vacuo to give 22.87 g of crude methanesulfonic acid 4-formylphenyl ester, which was used in the next step without further purification.
Workup
- waitleft at room temperature for 16 h
- extractionThe mixture was extracted with ethyl acetate (4×300 ml)
- washThe combined organic layers were washed with a 5% aqueous solution of sodium hydrogen carbonate (3×200 ml) and brine (100 ml)
- dry with materialThey were dried over magnesium sulphate
- customThe solvent was removed in vacuo
Sources & evidence
- ORD record
- ord-ed5a9dd1b28248f1aa16a6820ce1f5ce
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07101898B2
Reaction notes
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