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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798779Generated: October 31, 2026

Sodium borohydride → HCID 57887027, compound

https://huagongshe.com/reaction/1798779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57887028HCID 57887028—
SolventMethanolHCID 887—
ProductHCID 57887027HCID 5788702768%

Reaction Steps

Sodium borohydride (0.59 g, 15.6 mmol) was added portion wise to a stirred solution of 1,1-dimethylethyl 2-(2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}ethyl)-5-(4-iodophenyl)-3-oxopentanoate (7.55 g, 14.2 mmol) in methanol (100 mL) at 0° C. under nitrogen. On completion of addition stirring was continued for 1.5 h then the reaction was quenched with saturated aqueous ammonium chloride solution (100 mL). The resulting mixture was extracted with diethyl ether (3×200 mL) then the organic layers were combined, washed with brine (100 mL), dried (sodium sulfate) and the solvent evaporated. The residue was chromatographed on silica gel (25% to 50% diethyl ether: cyclohexane) to give the title compound (5.14 g, 68%) as a colourless oil which was a mixture of diastereomers. LC/MS: 4.72 min; z/e 535, calcd (M+1) 535. 1H NMR (400 MHz: CDCl3): 7.55 (2H), 6.95 (2H), 3.85-3.55 (3H), 3.30 (1H minor), 3.00 (1H major), 2.80 (1H), 2.65 (1H), 2.55 (1H major), 2.50 (1H minor), 1.95-1.65 (4H), 1.45 (9H), 0.90 (9H), 0.5 (6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343986B2
Source datasetuspto-grants-2013_01
ORD IDord-1a35492887d543f6a1ae5558c28c292b
Source noteuspto-grants-2013_01