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General procedure
for the reductive dehydroxylation of benzylic alcohols 4: Anhydrous
FeCl3 (2.4 mg, 0.015 mmol, 5 mol% equiv) was
carefully weighed and stirred in 1,2-dichloroethane (2 mL) for 5
min. PMHS (0.05 mL, 0.9 mmol, 3.0 equiv) was then added to the prepared
catalyst solution, followed by benzylic alcohol 4 (0.3
mmol, 1.0 equiv) and stirred at either r.t. or heated to the respective temperature.
The residual crude product was concentrated in vacuo and purified
by flash chromatography to afford the desired product 5. ¹H NMR and ¹³C
NMR data of previously unknown compounds: 4-heptyl-1,2-dimethoxybenzene
(5d). ¹H NMR (400 MHz,
CDCl3): δ = 7.26-6.70
(m, 3 H), 3.87 (s, 3 H), 3.85 (s, 3 H),
2.54 (t, J = 7.8 Hz,
2 H), 1.60-0.86 (m, 13 H); ¹³C
NMR (100 MHz, CDCl3): δ = 148.7, 147.0, 135.6,
120.1, 111.8, 111.2, 55.9, 55.8 35.6, 31.8, 31.7, 29.3, 29.2, 22.7,
14.1; HRMS (ESI): m/z [M + 1] calcd
for C15H25O2: 237.1855; found:
237.1850. 1-Bromo-4-heptyl-benzene (5k):¹¹ ¹H
NMR (400 MHz, CDCl3): δ = 7.37 (d, J = 8.3 Hz,
2 H), 7.03 (d, J = 8.3
Hz, 2 H), 2.54 (t, J = 7.8 Hz,
2 H), 1.63-1.53 (m, 2 H), 1.36-1.19
(m, 8 H), 0.88 (t, J = 6.8
Hz, 3 H); ¹³C NMR (100 MHz,
CDCl3): δ = 141.8, 131.2, 130.1, 119.2,
35.3, 31.8, 31.3, 29.1, 29.1, 22.6, 14.1; HRMS (ESI): m/z [M + 1] calcd
for C13H20Br: 255.0748; found: 255.0757.