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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289379Generated: October 31, 2026

Dichloromethane → Methyl (S)-3-benzyloxyheptanoate

https://huagongshe.com/reaction/2289379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantBenzyl 2,2,2-trichloroacetimidateHCID 144968—
Reactantmethyl (S)-3-hydroxyheptanoateHCID 10419468—
SolventCyclohexaneHCID 8078—
ProductMethyl (S)-3-benzyloxyheptanoateHCID 5435022484.5%

Reaction Conditions

Temperature22.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093345
Source datasetuspto-grants-2000_07
ORD IDord-cee57e8f3499411293a8ad1a3faa20a4
Source noteuspto-grants-2000_07