Table 3. Co–Mo–S-catalysed alkylation of benzenethiol (1a) with alcohols a .
| |||||||||
| Entry | Product | Conv. b [%] | Yield [%] |
Entry | Product | Conv. b [%] | Yield [%] |
||
| 3 c | 4a b | 3 c | 4a b | ||||||
| 1 |
|
>99 | 88 | 3 | 11 |
|
>99 | 93 | 2 |
| 2 |
|
>99 | 89 | — | 12 |
|
93 | 76 | 7 |
| 3 |
|
>99 | 96 | — | 13 d |
|
>99 | 73 | 9 |
| 4 |
|
>99 | 95 | — | 14 |
|
>99 | 79 | 13 |
| 5 |
|
>99 | 91 | — | 15 |
|
97 | 86 | 6 |
| 6 |
|
>99 | 82 | 11 | 16 |
|
>99 | 86 | 3 |
| 7 |
|
>99 | 84 | — | 17 |
|
94 | 81 | 3 |
| 8 |
|
>99 | 81 | — | 18 |
|
>99 | 87 | 9 |
| 9 |
|
82 | 51 | 15 | 19 |
|
92 | 81 | — |
| 10 |
|
95 | 80 | 8 | 20 |
|
>99 | 82 | 13 |
aReaction conditions: 1a (0.25 mmol), alcohol 2c–2v (0.5 mmol), Co–Mo–S-0.83 (13.1 mg), toluene (1.6 mL), 3.5 bar N2, 180 °C, 18 h.
bDetermined by GC with respect to 1a using n-hexadecane as an internal standard.
cYield of isolated products. GC-yield of by-products:
d 3aa (4%).