Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

82657-70-3

(4-propylphenyl)Methanol synthesis

11synthesis methods
-

Yield:82657-70-3 95%

Reaction Conditions:

with lithium aluminium tetrahydride in tetrahydrofuran;diethyl ether at 0 - 20; for 1 h;Inert atmosphere;

Steps:

96.1 Step 1. Preparation of (4-propylphenyl)-methanol

Under nitrogen atmosphere, at 0 °C, to a suspension of LiA1H4 (2.0 M THF solution,6.1 mL, 12.2 mmol) in dry Et20 (30 mL), 4-propylbenzoic acid (0.5 g, 3.05 mmol) in dry Et20(10 mL) was added dropwise. The resulting reaction mixture was stirred at r.t. for 1 h, and thencooled to 0 °C. H20 (0.50 mL) was slowly and cautiously added, followed by 3.0 M KOHsolution (0.50 mL) and additional H20 (2.2 mL). The mixture was stirred at 0 °C for 1 h and then filtered off. The organic layer was dried over Na2504, filtered and concentrated to dryness, affording the title compound (0.43 g, 95%), which was used in the next step without any further purification. R= 2.22 mi ‘HNMR(DMSO-d6): ? 7.22 (d, 2H, J= 7.9 Hz), 7.13 (d, 2H, J= 7.9Hz), 5.07 (t, 1H, J= 5.8 Hz), 4.46 (d, 2H, J= 5.8 Hz), 2.53 (t, 2H, J= 7.5 Hz), 1.56 (sex, 2H, J=7.5 Hz), 0.89 (t, 3H, J= 7.5 Hz).

References:

WO2014/144836,2014,A2 Location in patent:Paragraph 0965; 0966