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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819284Generated: November 1, 2026

Acetic Acid → HCID 86640928, compound

https://huagongshe.com/reaction/1819284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCerium trichloride heptahydrateHCID 21585214—
ReactantHCID 68587535HCID 68587535—
SolventEthanolHCID 702—
ProductHCID 86640928HCID 8664092835%

Reaction Steps

To a −78° C. solution of (3S, 4aS, 8aR) 6-oxo-2-tert-butoxycarbonyl-1,2,3,4,4a, 5,6,7,8,8a-decahydroisoquinoline-3-carboxylic acid (6.88 g, 21.14 mmol)(see Preparation 2, Steps A and B, below and Scheme III, Step A generally) and cerium trichloride heptahydrate (7.9 g, 21.2 mmol) in absolute ethyl alcohol (90 mL), under nitrogen sodium borohydride (1.24 g, 32.73 mmol) was added in portions. The resulting mixture was slowly warmed up to room temperature over 5 hours. The reaction mixture was cooled down to 0° C. and acetic acid (50% in water, 25 mL) was carefully added. The resulting mixture was stirred for 1 hour at room temperature and the solvent was removed in vacuo. To the resulting material water and ethyl acetate were added and the phases separated. Aqueous layer was extracted with ethyl acetate (3×). The combined organic phases were dried, filtered and concentrated in vacuo. Flash chromatography (silicagel, 70% ethyl acetate/hexane) gave ethyl (3S, 4aS, 6S, 8aR) 6-hydroxy-2-tert -butoxycarbonyl-1,2,3,4,4a, 5,6,7,8,8a-decahydroisoquinoline-3-carboxylate (2.4 g, 35%) and the title compound (4.15 g, 60%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601738B2
Source datasetuspto-grants-2009_10
ORD IDord-23ea305fb30645cfbabf56b167119d80
Source noteuspto-grants-2009_10