تفاعل #1833281

معادلة التفاعل

2-(hydroxymethyl)phenol

1-bromobutane

NaOH

→

title compound

المردود 77.7%

[2-(Butyloxy)phenyl]methanol

المردود 77.7%

المذيبات

ethanol

water

ظروف التفاعل

المعالجة

1. 1
   أخرىgiving a reaction time of 30 minutes
2. 2
   أخرىAfter all starting solutions had been consumed
3. 3
   أخرىthe system was purged with an additional 70 ml solvent (1:1, ethanol:water)
4. 4
   تركيزThe collected material was concentrated in vacuo
5. 5
   أخرىThe residue was partitioned between water and EtOAc
6. 6
   workup.ADDITIONtreated with saturated aqueous sodium bicarbonate solution
7. 7
   استخلاصThe aqueous phase was further extracted with EtOAc
8. 8
   أخرىthe combined organic extracts were dried (hydrophobic frit)
9. 9
   تركيزconcentrated in vacuo
10. 10
    أخرىThe residue was purified on silica (100 g)
11. 11
    تركيزconcentrated in vacuo

الإجراء التجريبي

A solution of 2-(hydroxymethyl)phenol (Aldrich; 1.24 g, 10 mmol) and 1-bromobutane (Acros; 1.18 ml, 11 mmol) in ethanol (5 ml) (total volume approximately 7 ml) was mixed in a flow reactor (Vapourtec R4, 30 ml PFA tubing, 110° C.) with a solution of aqueous NaOH (2 N, 5 ml, 10 mmol) in water (2 ml). The reagents were each pumped at 0.5 ml/min), giving a reaction time of 30 minutes. After the 30 ml reactor, the solution passed through a second “cooling” reactor (5 ml) at 50° C. At the reactor output, a 250 psi back pressure regulator was used. After all starting solutions had been consumed, the system was purged with an additional 70 ml solvent (1:1, ethanol:water). The collected material was concentrated in vacuo. The residue was partitioned between water and EtOAc, and treated with saturated aqueous sodium bicarbonate solution. The aqueous phase was further extracted with EtOAc, and the combined organic extracts were dried (hydrophobic frit) and concentrated in vacuo. The residue was purified on silica (100 g) using 0-100% ethyl acetate-cyclohexane. The appropriate fractions were combined and concentrated in vacuo to give the title compound (1.4 g); LCMS (System 4): MNH4+=198, tRET=2.51 min.

المصدر