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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45159Generated: October 29, 2026

Acetic Anhydride → HCID 67538732, compound

https://huagongshe.com/reaction/45159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium hydrideHCID 24758—
Reactant1H-Indole, 5-[[6-[(phenylmethoxy)methyl]-4-pyrimidinyl]oxy]-HCID 59394260—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67538732HCID 67538732—

Reaction Steps

To a solution of 5-(6-benzyloxymethyl-pyrimidin-4-yloxy)-1H-indole (12 g, 36.2 mmol) in THF (300 mL), NaH (1.74 g, 43.5 mmol) and acetic anhydride (5.13 mL, 54.3 mmol) are added. After 1 h the reaction is quenched with aqueous ammonium chloride and extracted with EtOAc. Most of the impurities are removed passing it through a silica gel column eluting with 50:50 heptane:EtOAc to give crude 1-[5-(6-benzyloxymethyl-pyrimidin-4-yloxy)-indol-1-yl]-ethanone. This is then dissolved in TFA (300 mL) and heated to 100° C. for 6 hours. At this point the solvent is removed and 1-[5-(6-hydroxymethyl-pyrimidin-4-yloxy)-indol-1-yl]-ethanone isolated via FCC eluting with EtOAc. MS (ESI) m/z 284.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541432B2
Source datasetuspto-grants-2013_09
ORD IDord-86d1f7e675fc4d5e9f2355eaaea053c6
Source noteuspto-grants-2013_09