HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289379Generated: October 31, 2026
Dichloromethane → Methyl (S)-3-benzyloxyheptanoate
https://huagongshe.com/reaction/2289379
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Benzyl 2,2,2-trichloroacetimidate | HCID 144968 | — |
| Reactant | methyl (S)-3-hydroxyheptanoate | HCID 10419468 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Methyl (S)-3-benzyloxyheptanoate | HCID 54350224 | 84.5% |
Reaction Steps
In a 2 flask were charged 275 ml of methylene chloride, 550 ml of cyclohexane, 140 g of benzyl trichloroacetoimidate, and 75 g of methyl (S)-3-hydroxyheptanoate (compound (37), R1 =ethyl), and 6 ml of trifluoromethanesulfonic acid was added thereto over 5 minutes while maintaining at 20 to 25° C., followed by allowing the mixture to react at 35 to 40° C. for 5 hours. The by-produced salt was removed by filtration, and the filtrate was washed with a sodium hydrogencarbonate aqueous solution. The solvent was removed by distillation under reduced pressure, and the residue was distilled under reduced pressure to obtain 99.0 g (78.7%) of the titled compound (b.p.: 105-108° C./0.1 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06093345 |
|---|
| Source dataset | uspto-grants-2000_07 |
|---|
| ORD ID | ord-cee57e8f3499411293a8ad1a3faa20a4 |
|---|
| Source note | uspto-grants-2000_07 |
|---|