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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067206Generated: November 1, 2026

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

https://huagongshe.com/reaction/1067206

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 9, 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 vacua 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) δ1.44 (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), 7.30 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248717B1
Source datasetuspto-grants-2001_06
ORD IDord-501db7101d8f40dd8fa3e4739b11e789
Source noteuspto-grants-2001_06