(Phenylmethoxy)acetaldehyde → HCID 19922573, compound

To a solution of 21.5 mg (0.05 mmol) of (R)-1 in 3 ml of toluene were added 176 mg (1 mmol) of 1-ethylthio-1-(trimethylsilyl)oxyethene and 150 mg (1 mmol) of α-benzyloxyacetaldehyde at 0° C. After stirring for 2 hours at that temperature, the resultant mixture was poured into 10 ml of a buffer (pH 7) at 0° C. The solution was filtered through a pad of Celite, and the filtrate was extracted three times with a 5 ml portion of diethyl ether. The combined organic layer was washed with brine, dried over magnesium sulfate, and evaporated under reduced pressure to give a crude product in a silylated form. The crude product was poured into 10% hydrochloric acid-methanol, and the mixture was purified by silica gel chromatography (eluent: hexane/ethyl acetate=20/1 by volume) to obtain S-ethyl 4-benzyloxy-3-hydroxybutanethioate in a yield of 84%.

1. filtrationThe solution was filtered through a pad of Celite
2. extractionthe filtrate was extracted three times with a 5 ml portion of diethyl ether
3. washThe combined organic layer was washed with brine
4. dry with materialdried over magnesium sulfate
5. customevaporated under reduced pressure
6. customto give a crude product in a silylated form
7. customthe mixture was purified by silica gel chromatography (eluent: hexane/ethyl acetate=20/1 by volume)

ORD record

ord-e81ec7534ad64f2ebc1bd3092117ca4a

Source dataset

uspto-grants-1995_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05434289