Benzaldehyde → HCID 21417747, compound
Reaction equation
[SH:1][CH2:2][CH2:3][CH:4]([OH:6])[CH3:5].[CH:7](=O)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(NCC)C>ClCCl>[CH3:5][CH:4]1[O:6][CH:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[S:1][CH2:2][CH2:3]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
75 ml of dichloromethane is placed into a 100 ml round-bottom flask. To the dichloromethane is added 5.3 grams (0.05 moles) of 4-mercapto-2-butanol. 5.8 grams (0.055 moles) of benzaldehyde is then added followed by 0.1 grams of p-toluene sulfonic acid. Boiling chips are added to the flask. A Dean-Starke distilling receiver is placed on the flask, and a reflux condenser is placed on the receiver. The flask is then heated slowly until reflux occurs, and then the temperature is increased for a more vigorous reflux. The reflux lasts for a period of 2 hours before water of reaction ceases to be formed. The reaction mass is then cooled and neutralized with diethyl amine to a pH of 8. The reaction mass is filtered through fluted filter paper, and the dichloromethane solvent is removed by means of rotary evaporation. 10.1 grams of crude product are recovered after the rotary evaporation operation. The crude product is then distilled by means of vacuum distillation yielding the following 3 fractions:
Workup
- additionBoiling chips are added to the flask
- distillationA Dean-Starke distilling receiver
- temperatureThe flask is then heated slowly
- temperatureuntil reflux
- temperaturethe temperature is increased for a more vigorous reflux
- customThe reflux lasts for a period of 2 hours before water of reaction ceases
- customto be formed
- temperatureThe reaction mass is then cooled
- filtrationThe reaction mass is filtered
- filtrationthrough fluted filter paper
- customthe dichloromethane solvent is removed by means of rotary evaporation
- custom10.1 grams of crude product are recovered after the rotary evaporation operation
- distillationThe crude product is then distilled by means of vacuum distillation
- customyielding the following 3 fractions
Sources & evidence
- ORD record
- ord-86e09dba1931446f8483a2cd6756c9ae
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04031257
Reaction notes
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