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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545625Generated: October 29, 2026

Acetic Acid → HCID 57670737, compound

https://huagongshe.com/reaction/545625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl 4-FormylbenzoateHCID 15294—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 42599086HCID 42599086—
SolventDichloromethaneHCID 6344—
ProductHCID 57670737HCID 5767073719.7%

Reaction Steps

To a solution of 2-[4-(hexahydro-pyrrolo[3,4-c]pyrrol-2-ylmethyl)-phenoxy]-benzothiazole (200 mg, 0.56 mmol) in CH2Cl2 (22 mL) was added 4-formyl-benzoic acid methyl ester (103 mg, 0.62 mmol) followed by the addition of acetic acid (28 μL, 0.48 mmol) then sodium triacetoxyborohydride (144 mg, 0.68 mmol). The reaction stirred at rt for 16 h. The reaction was then washed with satd. aq. NaHCO3 (2×20 mL). The organic layer was dried, filtered and concentrated. The resulting oil was purified by column chromatography (20% to 60% EtOAc in Hexanes) to afford the title compound (55 mg, 19%). MS (ESI): mass calcd. for C29H29N3O3S, 499.64; m/z found, 500.2 [M+H]+. 1H NMR (500 MHz, CDCl3): 8.01 (d, J=8.3 Hz, 2H), 7.76 (d, J=8.1 Hz, 1H), 7.47-7.38 (m, 1H), 7.35-7.26 (m, 4H), 7.68 (d, J=7.9 Hz, 4H), 3.92 (s, 4H), 3.65 (d, J=12.2 Hz, 4H), 2.71-2.60 (m, 3H), 2.38 (d, J=7.2 Hz, 4H), 1.27 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935725B2
Source datasetuspto-grants-2011_05
ORD IDord-769de1f5eaf2475b90498d599b8fc16a
Source noteuspto-grants-2011_05