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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689208Generated: October 25, 2026

Triethylamine → 2-Methylpentane

https://huagongshe.com/reaction/1689208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Methylthiophene-2-carboxylic acidHCID 74713—
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantTert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochlorideHCID 66964240—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-MethylpentaneHCID 7892—
ProductTert-butyl 4-(5-methylthiophene-2-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 57989101—

Reaction Steps

1-Propanephosphonic acid cyclic anhydride (1.57M solution in THF, 0.64 mL) was added to a solution of tert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochloride (WuXi PharmaTech) (0.26 g), 5-methylthiophene-2-carboxylic acid (0.142 g) and triethylamine (0.84 mL) in DMF (8 mL) and the resulting mixture stirred for 16 h. The reaction mixture was poured into water (100 mL) and extracted with ethyl acetate (3×200 mL). The combined organic solutions were washed with water (2×100 mL) and brine (100 mL), then dried over magnesium sulphate, filtered and evaporated in vacuo. Purification was by silica gel chromatography eluting with ethyl acetate:isohexane, 1:1 to give the subtitled compound as a clear oil. Yield 0.32 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-2bea720a39d74bf59b258f8b62f8270c
Source noteuspto-grants-2012_04