HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-bromooctanoyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Octanoic acid, 2-bromo- | HCID 552003 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-bromooctanoyl Chloride | HCID 11075607 | 64% |
Reaction Steps
To a solution of 20 g (90 mmol) 2-bromooctanoic acid in 100 mL toluene was added 13.2 mL (180 mmol) thionyl chloride. The solution was heated at reflux under nitrogen for 3 hours. The excess thionyl chloride and toluene were distilled at atmospheric pressure under N2. The yellow residue was purified by kugelrohr distillation (bp=60°-65° C./0.1 mm Hg) and 13.8 g (64%) of the 2-bromooctanoyl chloride as a colorless oil was isolated. 1H NMR (CDCl3)δ0.85-0.95 (m,3H,CH3), 1.24-1.57 (m,8H,CH2), 1.98-2.22 (m,2H,CH2CBr) 4.51 (t, J=7.10 Hz, 1H, CHBr); IR (CHCl3) 1788 (C=O) cm-1 ; microanalysis: calcd. for C8H14BrClO-39.78% C,5.84% H, 33.08% Br, 14.68% Cl, found-39.55% C,5.91% H, 33.17% Br, 14.84% Cl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05274143 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-1572eda819384e7292d336dbbf2736d5 |
| Source note | uspto-grants-1993_12 |