Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389191Generated: November 2, 2026

Trifluoroacetic acid → HCID 178464331, compound

https://huagongshe.com/reaction/2389191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178447442HCID 178447442—
ReactantHCID 178464334HCID 178464334—
ProductHCID 178464331HCID 17846433156%

Reaction Steps

4-Amino-4-[5-trifluoromethyl-6-(trans-4-trifluoromethyl-cyclohexyloxy)-naphthalen-2-yl]-pentanoic acid was synthesized as per 4-amino-4-[6-(trans-4-trifluoromethyl-cyclohexyloxy)-naphthalen-2-yl]-pentanoic acid (Example 282) in 56% yield (as TFA salt), using 4-nitro-4-[5-trifluoromethyl-6-(trans-4-trifluoromethyl-cyclohexyloxy)-naphthalen-2-yl]-pentanoic acid as starting material. MS: m/z=500.20 [M+Na]+. 1H NMR (400 MHz, DMSO-d6) δ ppm: 12.23 (br. s., 1H), 8.53 (br. s., 3H), 8.22 (d, J=9.3 Hz, 1H), 8.12 (d, J=8.0 Hz, 1H), 8.05 (d, J=1.5 Hz, 1H), 7.72-7.80 (m, 2H), 4.62-4.73 (m, 1H), 2.35-2.42 (m, 1H), 2.21-2.34 (m, 2H), 2.07-2.20 (m, 3H), 1.88-2.05 (m, 3H), 1.66-1.78 (m, 3H), 1.40-1.60 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269043B2
Source datasetuspto-grants-2012_09
ORD IDord-2c8f19c6ca854651adafbb96a080ade6
Source noteuspto-grants-2012_09