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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533461Generated: October 31, 2026

Benzaldehyde → HCID 9838153, compound

https://huagongshe.com/reaction/1533461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
Reactant1-Ethoxy-2,3-DifluorobenzeneHCID 2782928—
ReactantHCID 178506865HCID 178506865—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 9838153HCID 9838153—

Reaction Steps

1.1 kg/h of a 1 M solution of 2,3-difluorophenetole containing 10 mol % of 2,2,6,6-tetramethylpiperidine were introduced into a continuous-flow reactor and mixed with 0.4 kg/h of a 2.5 M solution of hexyllithium in hexane at −35° C. After the mixture had passed through the reaction zone, 0.28 kg/h of a 4.7 M solution of benzaldehyde in THF was mixed in. After the reaction had finished, the product was collected and worked up in the customary manner, giving 2,3-difluoro-4-ethoxy-α-phenylbenzyl alcohol. The conversion based on the starting compound was 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207835B1
Source datasetuspto-grants-2001_03
ORD IDord-2c79ef8fe2e94c688b9316149898a8f1
Source noteuspto-grants-2001_03