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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53452Generated: October 30, 2026

Sodium Chloride → 17beta-(3,4-Methylenedioxybenzoyl)-estra-1,3,5(10)-triene-3-carboxylic acid

https://huagongshe.com/reaction/53452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
Reactant17beta-(3,4-Methylenedioxybenzoyl)-estra-1,3,5(10)-triene-3-carboxaldehydeHCID 86750697—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product17beta-(3,4-Methylenedioxybenzoyl)-estra-1,3,5(10)-triene-3-carboxylic acidHCID 5381814547%

Reaction Steps

To a stirred mixture of 17β-(3,4-methylenedioxybenzoyl)-estra-1,3,5(10)-triene-3-carboxaldehyde (0.041 g, 0,1 mmoles), tert-butyl alcohol (1.05 mL), 2-methyl-2-butene (4 mL of 2M solution in THF, 8 mmoles) at 0° C. was added a solution of NaClO2 (9 mg, 0.1 mmoles) and NaH2PO4. H2O (0.137 g, 0.1 mmoles) in H2O (0.4 ml) and stirred for 2 hours at ambient temperature. Acetic acid (glacial, 0.8 ml) and saturated NaCl solution (1.3 mL) were added to the reaction mixture which was extracted with EtOAc. The organic layer was washed with H2O, brine, dried (MgSO4), concentrated and azetroped with toluene. The resulting solid was triturated with CH3CN- acetone and filtered to give 0.02 g (47%) of the title compound as a white solid, mp 235°-237° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618806
Source datasetuspto-grants-1997_04
ORD IDord-445fe49cda48466b98b98166a74cd334
Source noteuspto-grants-1997_04