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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292653Generated: October 30, 2026

2-Methylbenzenesulfonic acid hydrate → HCID 131719382, compound

https://huagongshe.com/reaction/1292653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzenesulfonic acid hydrateHCID 12496995—
ReactantHCID 131719383HCID 131719383—
SolventMethanolHCID 887—
ProductHCID 131719382HCID 13171938289.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of N-[O-[(1,1-dimethylethyl)-dimethylsilyl]-N-[(phenylmethoxy)carbonyl]-L-homoseryl]-O-(2,2-dimethoxyethyl)-L-serine, methyl ester [5.56 g, 10 mmol, prepared as described in Example 10(h)] in methanol (65 ml) was cooled to 0° C. (ice salt bath), treated with p toluenesulfonic acid monohydrate (386 mg, 2.0 mmol) and stirred at 0° C. for 1.5 hours. The reaction was quenched with sodium bicarbonate solution (198 mg. in 20 ml water), stirred for 5 minutes then evaporated to remove the methanol. The aqueous phase was extracted with ethyl acetate (2×200 ml) and the combined organic extract was washed with water (110 ml), 5% sodium bicarbonate (80 ml) and brine (80 ml), dried (anhydrous sodium sulfate), filtered, evaporated to dryness and dried in vacuo. The crude product was chromatographed on silica gel column (Merck), eluting the column with ethyl acetate:hexane (2:1) and ethyl acetate:methanol (98:2) to give 3.975 g of title product as a syrup. TLC (ethyl acetate:hexane, 4:1) Rf =0.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05756832
Source datasetuspto-grants-1998_05
ORD IDord-d7eea999ca244c0f8410121aa8bce927
Source noteuspto-grants-1998_05