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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376005Generated: October 30, 2026

Ammonium Chloride → beta(R)-benzyloxy-alpha(RS)-phenyl-1,4-dioxaspiro[4,5]decane-2(R)-ethanol

https://huagongshe.com/reaction/376005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactantalpha(S)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-acetaldehydeHCID 22856132—
ReactantHCID 178478979HCID 178478979—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Productbeta(R)-benzyloxy-alpha(RS)-phenyl-1,4-dioxaspiro[4,5]decane-2(R)-ethanolHCID 22856134—

Reaction Conditions

Temperature-5 °C

Reaction Steps

A solution of 4.30 g (0.015 mmol) of α(S)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-acetaldehyde in 50 ml of anhydrous diethyl ether was cooled to -8° C. and 15 ml of a 2M solution of phenylmagnesium chloride in tetrahydrofuran were added dropwise over a period of 1 hour. The mixture was stirred at -5° C. for 2 hours, then allowed to warm to room temperature and poured into 50 ml of 10% ammonium chloride solution. The mixture was extracted twice with 100 ml of ethyl acetate each time. The ethyl acetate extracts were dried over anhydrous magnesium sulphate and evaporated. The residue was subjected to flash chromatography on silica gel using 5% methanol in dichloromethane for the elution. There were obtained 2.47 g of β(R)-benzyloxy-α(RS)-phenyl-1,4-dioxaspiro[4,5]decane-2(R)-ethanol in the form of a colourless gum; MS (C.I.): m/e 369 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05488115
Source datasetuspto-grants-1996_01
ORD IDord-36ba96c85f274e85b2dd314a3c03b28f
Source noteuspto-grants-1996_01