HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenylcyclohexyl 4-methylbenzenesulfonate → HCID 178419141, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenylcyclohexyl 4-methylbenzenesulfonate | HCID 13586894 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178419150 | HCID 178419150 | — |
| Product | HCID 178419141 | HCID 178419141 | — |
Reaction Steps
The product is made similarly to its analog in Example 1 from dicyclopentyl-phosphine-borane (10.6 g; 57.5 mmol.), n-butyl lithium (39.5 mL of 1.6 M solution; 63.3 mmol.) and 4-phenylcyclohexyl 4-methylbenzenesulfonate (22.8 g; 68.9 mmol.). Yield 14.5 g (74%). 31P{1H} NMR (δ, C6D6, ppm): 33.22 and 33.83 (broad); 1H NMR (δ, C6D6, ppm): 0.944 (m, 3H, BH3), 1.2-2.2 (m, 27H, cyclopentyl+cyclohexyl), 2.82 (m, 1H, PhCH), 7.0-7.25 (m, 5H, Ph).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466306B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-8bd30be6265f4771953abb47a08b3a3b |
| Source note | uspto-grants-2013_06 |