HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 57835390, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 57835418 | HCID 57835418 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57835390 | HCID 57835390 | 62% |
Reaction Steps
A solution of 1-{4-[1-ethyl-1-(5-hydroxy-benzo[b]thiophen-2-yl)-propyl]-2-methyl-phenoxy}-3,3-dimethyl-butan-2-one (260 mg, 0.612 mmol) in CH2Cl2 (20 mL) at RT is treated with Et3N (0.40 mL) and methanesulfonyl chloride (140 mg, 1.22 mmol). The mixture is stirred for 30 min and quenched with water (1.0 mL). The organic layer is concentrated and purified using silica gel column chromatography (25% EtOAc/Hex) to afford the title compound (190 mg, 62%). NMR (ppm, CDCl3), δ: 7.67 (1 H, d, J=8.8 Hz), 7.59 (1 H, d, J=2.2 Hz), 7.13 (1 H, dd, J=2.2, 8.8 Hz), 7.11 (1 H, s), 7.01-7.04 (2 H, m), 6.51 (1 H, d, J=8.4 Hz), 4.84 (2 H, s), 3.16 (3 H, s), 2.26 (3 H, s), 2.15 (4 H, q, J=7.5 Hz), 1.26 (9 H, s), 0.74 (6H, t, J=7.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582775B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-fe2e8c109c5a47928b5b0871bba1f4c1 |
| Source note | uspto-grants-2009_09 |