HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53928Generated: October 25, 2026
Thionyl Chloride → 4-(Chloromethyl)-2-(propan-2-yl)-1,3-oxazole
https://huagongshe.com/reaction/53928
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Chloromethyl-4-hydroxy-2-isopropyoxazoline | HCID 10749814 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(Chloromethyl)-2-(propan-2-yl)-1,3-oxazole | HCID 2763291 | 96% |
Reaction Steps
A solution of 4-chloromethyl-4-hydroxy-2-isopropyloxazoline (4.88 g, 0.0275 mol) in 1,2-dichloroethane (20 mL) was added to a solution of SOCl2 (2.40 mL, 0.0329 mol)in 1,2-dichloroethane (80 mL) at 0° C. under argon, and the solution was heated to 70° C. After 15 min at 70° C., the reaction was cooled to room temperature and the solvent removed by rotary evaporation in vacuo. Drying the residue on high vacuum gave the desired compound as a brown semi-solid (4.20 g, 0.0263 mol, 96%): 1H NMR (CDCl3) δ 1.36 (d, J=7.5 Hz, 6H), 3.03-3.18 (m, 1H), 4.50 (s, 2H), 7.56 (s, 1H). Mass spectrum: (M+H)+ =160, 162.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05621109 |
|---|
| Source dataset | uspto-grants-1997_04 |
|---|
| ORD ID | ord-6c53a1862e104e9882f1032a9ff2f155 |
|---|
| Source note | uspto-grants-1997_04 |
|---|