HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 14986648, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-{[tert-Butyl(dimethyl)silyl]oxy}hexanoic acid | HCID 12717311 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 14986648 | HCID 14986648 | 92% |
Reaction Steps
A solution of 0.5 g (2.03 mmol) of 6-[(tert-butyldimethylsilyl)oxy]-hexanoic acid in 4 ml of benzene is mixed with 362 mg (3.04 mmol, 1.5 equivalents) of SOCl2 and heated under reflux for 2 hours. It is allowed to cool, and the solvent is distilled off in a rotary evaporator. To remove excess SOCl2 from the reaction mixture, the residue is mixed again with benzene and again distilled off. 494 mg (1.865 mmol, 92%) of the 6-[(tert-butyldimethylsilyl)oxy]-hexanoyl chloride is obtained. This crude product is further reacted without purification and characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05969145 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-39bcfc28f2d84ced9c19de69e2b00cf0 |
| Source note | uspto-grants-1999_10 |