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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188218Generated: October 25, 2026

1,8-Octanediol → (R)-3-[8-(2-fluoro-4-trifluoromethyl-benzyloxy)-octanoylamino]-4-dimethylamino-butyric acid benzyl ester

https://huagongshe.com/reaction/1188218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-OctanediolHCID 69420—
Reactant2-Fluoro-4-(trifluoromethyl)benzyl bromideHCID 2737570—
Reactant(R)-benzyl 3-amino-4-(dimethylamino)butanoate dihydrochlorideHCID 46223507—
Reactant8-(2-Fluoro-4-trifluoromethyl-benzyloxy)-octan-1-olHCID 66874749—
Reactant8-(2-Fluoro-4-trifluoromethyl-benzyloxy)-octanoic acidHCID 66874977—
Product(R)-3-[8-(2-fluoro-4-trifluoromethyl-benzyloxy)-octanoylamino]-4-dimethylamino-butyric acid benzyl esterHCID 66874965—

Reaction Steps

The title compound, m/e=463.1 ([M−H]−), was produced in analogy with intermediate 1, steps 1 to 4. Thus, 1,8-octanediol was alkylated in step 1 with 2-fluoro-4-trifluoromethyl-benzyl bromide, leading to 8-(2-fluoro-4-trifluoromethyl-benzyloxy)-octan-1-ol, which was oxidized in step 2 to 8-(2-fluoro-4-trifluoromethyl-benzyloxy)-octanoic acid. This was coupled in step 3 with (R)-3-amino-4-dimethylamino-butyric acid benzyl ester dihydrochloride to produce (R)-3-[8-(2-fluoro-4-trifluoromethyl-benzyloxy)-octanoylamino]-4-dimethylamino-butyric acid benzyl ester, which was hydrogenated in step 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673946B2
Source datasetuspto-grants-2014_03
ORD IDord-0aacf0e840784a59aa00213b9fdfb8f0
Source noteuspto-grants-2014_03