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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986993Generated: October 29, 2026

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

https://huagongshe.com/reaction/986993

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. The reaction mixture was partitioned between 4.5 L H2O and 4.5 L IPE. The layers were saparated and the pH of the aqueous layer was adjusted 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), 7.30 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630487B2
Source datasetuspto-grants-2003_10
ORD IDord-1f1cb1dfe6ad49f7937c0f0917f948f5
Source noteuspto-grants-2003_10