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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402769Generated: October 25, 2026

Acetic Acid → Methyl 4-{8-[(4-methyl-5-trifluoromethyl-2-bromophenyl)methyl]-2-oxo-1-oxa-3,8-diazaspiro[4.5]dec-3-yl}benzoate

https://huagongshe.com/reaction/402769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 4-(2-oxo-1-oxa-3,8-diazaspiro[4.5]dec-3-yl)benzoate hydrochloride saltHCID 66764605—
Reactant2-Bromo-4-methyl-5-(trifluoromethyl)benzaldehydeHCID 77230859—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-{8-[(4-methyl-5-trifluoromethyl-2-bromophenyl)methyl]-2-oxo-1-oxa-3,8-diazaspiro[4.5]dec-3-yl}benzoateHCID 6676464164.2%

Reaction Steps

To a solution of 2-bromo-4-methyl-5-trifluoromethylbenzaldehyde (100 mg, 0.374 mmol) in DMF (3 mL) was added methyl 4-(2-oxo-1-oxa-3,8-diazaspiro[4.5]dec-3-yl)benzoate (122 mg, 0.374 mmol) (from Example 1-1, Step 2) and DIPEA (0.326 mL, 1.87 mmol). The mixture was stirred at room temperature for 15 minutes and then acetic acid (0.107 mL, 1.87 mmol) and sodium triacetoxyborohydride (120 mg, 0.562 mmol) were added. The reaction was stirred at room temperature and was followed by LC/MS until complete. Water was added and the mixture was extracted twice with ethyl acetate. The organic layers were combined and dried over sodium sulfate and evaporated. The residue was purified on silica gel (CombiFlash 4 gm pre-packed column) eluting with a 10-30% ethyl acetate/hexanes gradient to afford the title intermediate (130 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742110B2
Source datasetuspto-grants-2014_06
ORD IDord-ea8c865b88b64468a5374d07af08274d
Source noteuspto-grants-2014_06