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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358695Generated: November 3, 2026

1-(Bromomethyl)-2,4-difluorobenzene → HCID 22557094, compound

https://huagongshe.com/reaction/1358695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-2,4-difluorobenzeneHCID 90297—
Reactant(R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acidHCID 637603—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22557094HCID 2255709471%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-Boc-(D)-serine (452 g, 2.2026 mol) in a mixture of THF (7 L) and DMF (3 L) at about 0° C. was added potassium tert-butoxide solution (515.8 g, 4.5963 mol). The reaction mixture was stirred at about 0° C. for about 30 min., then 2,4-difluorobenzyl bromide (456.5 g, 2.2051 mol) was added. After warming to room temperature, the reaction mixture was concentrated in vacuo to remove the THF. Partitioned the reaction mixture between 4.5 L H2O and 4.5 L IPE. Separated the layers and adjusted the pH of the aqueous layer with 1 N HCl to about 3. The aqueous layer was extracted twice with 4 L each of IPE. The organic solution was dried over Na2SO4, and concentrated in vacuo to yield a yellow waxy solid (518.0 g, yield: 70.9%). 1H-NMR (CDCl3) δ 1.44 (s, 9H), 3.73 (m, 1H), 3.94 (d, 1H), 4.44 (br s, 1H), 4.54 (s, 2H), 5.34 (m, 1H), 6.78 (m, 1H), 6.84 (m, 1H), 730 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596867B2
Source datasetuspto-grants-2003_07
ORD IDord-64c535d5f2ed44df9046e7ce9be27365
Source noteuspto-grants-2003_07