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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568878Generated: October 31, 2026

Sodium Bicarbonate → HCID 53794764, compound

https://huagongshe.com/reaction/568878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3,5-DibenzyloxybenzaldehydeHCID 561351—
ReactantPhosphonium, [3-(1-methoxy-1-methylethoxy)propyl]triphenyl-, bromideHCID 10950828—
ReactantButyllithiumHCID 178418339—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53794764HCID 5379476458.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred suspension of [3-(1-methoxy-1-methylethoxy)propyl](triphenylphosphonium)bromide (4 g) in dry THF (25 ml) at 0° C. was heated with butyl lithium (5.28 ml) and the mixture stirred at 0° C. for 10 min. 3,5-Bis(phenylmethoxy)benzaldehyde (2.24 g) in dry THF (15 ml) was added and the mixture stirred for a further 45 min at room temperature under nitrogen, diluted with ER (100 ml) and filtered through silica (20 g) twice. The filtrate was evaporated in vacuo to give a yellow oil which was dissolved in a mixture of THF (50 ml), water (5 ml) and 2M hydrochloric acid (1 ml) and left at room temperature for 30 min. The mixture was basified with sodium bicarbonate solution and extracted with ER (200 ml). The organic phase was washed with water (150 ml), brine (100 ml), dried and evaporated in vacuo to give a yellow oil. Purification by FCC eluting with ER-CX (3:2) gave a colourless oil (1.48 g). T.l.c. (ER-CX 3:1) Rf 0.26

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04730008
Source datasetuspto-grants-1988_03
ORD IDord-004c6c7d24d5455488fd82eeb388077e
Source noteuspto-grants-1988_03