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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565724Generated: October 30, 2026

(S)-mandelic acid → HCID 70239495, compound

https://huagongshe.com/reaction/565724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-mandelic acidHCID 439616—
ReactantHCID 70239410HCID 70239410—
Solventtert-Butyl methyl etherHCID 15413—
Product(S)-mandelic acidHCID 439616—
ProductHCID 70239495HCID 7023949557.2%

Reaction Steps

Methyl N-[(S)-α-methylbenzyl]-(RS)-pipecolate (157 mg) was dissolved in methyl tert-butyl ether (2 ml) at room temperature. To this solution was added a mixture of L-(+)-mandelic acid (86 mg) and methyl tert-butyl ether (2 ml) at room temperature and stirred. The resulting solution was allowed to stand at −20° C. for one day to form a crystal. The crystals were separated by filtration and dried to yield an L-(+)-mandelic acid salt of methyl N-[(S)-α-methylbenzyl]-(S)-pipecolate (79.9 mg) in an optical purity of 73% de and a yield of 23%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172234B2
Source datasetuspto-grants-2001_01
ORD IDord-a781dfaa67ff4b8f983fabb696471456
Source noteuspto-grants-2001_01