HCID 53859634, compound → HCID 53920932, compound

Participants

Reaction Steps

Using a similar procedure to that described in Example 1 for the preparation of ethyl 3-(3-allyl-4-trifluoromethylsulphonyloxyphenyl)propionate but using 3-(2-allyl-4-hydroxyphenyl)-1-methoxypropane as starting material there was obtained 2-allyl-4-(3-methoxypropyl)phenyl trifluoromethane sulphonate as a colourless oil; NMR(CDCl3): 1.8-1.95(2H,m), 2.65-2.75(2H,t), 3.3-3.5(7H,m), 5.05-5.2(2H,m), 5.8-6.0(1H,m) and 7.0-7.3(3H,m).

Provenance & Evidence