HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362270Generated: October 29, 2026
Methylamine → (3-Chloro-2-isopropoxybenzyl)methylamine
https://huagongshe.com/reaction/1362270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Chloro-2-isopropoxybenzaldehyde | HCID 59277602 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Chloro-2-isopropoxybenzyl)methylamine | HCID 66967106 | 93% |
Reaction Steps
Methylamine (10.3 mL of a 2.0 M solution in MeOH, 20.6 mmol) was added to 3-chloro-2-isopropoxybenzaldehyde (0.500 g, 2.52 mmol) and the mixture was stirred for 72 h. The solution was concentrated under reduced pressure. The resulting light yellow oil was dissolved in EtOH (10.3 mL) and treated with NaBH4 (0.095 g, 2.52 mmol). After stirring for 18 h, the reaction mixture was concentrated under reduced pressure, dissolved in 1 N NaOH (20 mL) and extracted with Et2O (3×50 mL). The combined organics were washed with brine (2×75 mL), dried (Na2SO4) and concentrated to give the title compound (0.50 g, 93%) as a yellow oil: 1H NMR (300 MHz, DMSO-d6) δ 7.40-7.31 (m, 2H), 7.08 (t, J=7.8 Hz, 1H), 4.42 (q, J=6.1 Hz, 1H), 3.66 (s, 2H), 2.25 (s, 3H), 2.02 (br s, 1H), 1.25 (d, J=6.1 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07879872B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-f9ee577666b54ade86bf7b28ecbd10b9 |
|---|
| Source note | uspto-grants-2011_02 |
|---|