HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 57658756, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 57658727 | HCID 57658727 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57658756 | HCID 57658756 | — |
Reaction Steps
To a solution of [4-bromo-2-(3-trimethylsilanylpropynoyl)phenoxy]acetic acid ethyl ester (0.83 g, 2.16 mmol) in methanol (20 mL) was added a 0.1M aqueous solution of Na2B4O7 (10 mL). After stirring for 2-3 minutes at room temperature, Et2O and 1N aq. HCl were added. The phases were separated, and the organic phase was washed with brine, dried (MgSO4) and concentrated in vacuo to give the title compound as yellow oil which crystallized upon standing (0.65 g, 2.09 mmol, 96%). LC/MS (an 10p8) Rt 3.58 min, m/z 311 [M+H]+; 1H NMR (CDCl3): δ1.31 (t, 3H), 3.45 (s, 1H), 4.27 (q, 2H), 4.74 (s, 2H), 6.83 (d, 1H), 7.61 (dd, 1H), 8.14 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022063B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-77e1e4ca6c66409f8ae563a181929b1c |
| Source note | uspto-grants-2011_09 |