HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 21069967, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 21069793 | HCID 21069793 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21069967 | HCID 21069967 | 96% |
Reaction Steps
Reaction of intermediate 9, 2-(2-(methylthio)ethoxy)propanoic acid, (13.70 g, 0.083 mol) with oxalyl chloride followed by reaction with methanol gave 14.27 g (96% yield) of the title ester as a clear oil; bp 55–60° C./0.3 torr (bulb to bulb distillation, air bath temperature). 1HNMR 400 MHz (CDCl3) δ ppm: 1.42 (3H, d, J=7.0 Hz, CH3), 2.15 (3H, s, SCH3), 2.71 (2H, t, J=6.8 Hz, CH2), 3.56 (1H, m, CH), 3.75 (3H, s, OCH3), 3.78 (1H, m, CH), 4.15 (1H, q, J=7.0 Hz, OCH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157447B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-041bdc13666a4552b946fd03dd212cad |
| Source note | uspto-grants-2007_01 |