HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 178459251, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Reactant | HCID 178501118 | HCID 178501118 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178459251 | HCID 178459251 | 39.2% |
Reaction Steps
To a solution of trans-methyl 4-(aminomethyl)cyclohexanecarboxylate (1 g, 5.8 mmol) in THF (50 mL) was added dropwise methylmagnesium bromide (7.7 mL, 23.2 mmol) at −78° C. The mixture was stirred at room temperature for 2 h. TLC (PE:EA=5:1) showed the reaction was complete. The mixture was quenched by the addition of NH4Cl (100 mL) and extracted with EtOAc (100 mL×3). The combined extracts were dried over Na2SO4, filtered and concentrated in vacuo to give 2-(trans-4-(aminomethyl)cyclohexyl)propan-2-ol (0.42 g, 39.2%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09416132B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-f63658df14b44c2da1a8e4a8841c34f9 |
| Source note | uspto-grants-2016_08 |