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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzenesulfonic acid hydrate | HCID 12496995 | — |
| Reactant | HCID 131719383 | HCID 131719383 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131719382 | HCID 131719382 | 89.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756832 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-d7eea999ca244c0f8410121aa8bce927 |
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| Source note | uspto-grants-1998_05 |
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