HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236147Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 11259454, compound
https://huagongshe.com/reaction/2236147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Boc-Tyr-OMe | HCID 7019130 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11259454 | HCID 11259454 | 93.4% |
Reaction Steps
N-Boc-L-tyrosine methyl ester 3 (103 g, 0.35 mol) and tosyl chloride (66.7 g, 0.35 mol) were dissolved in toluene (517 g) and then cooled to 0° C. To the mixture was added dropwise triethylamine (35.5 g, 0.35 mol) at 0° C. over 90 min. The mixture was further kept at 0° C. for 4 hrs. The reaction mass was washed with 5% hydrochloric acid (255 g) and 5% aqueous sodium bicarbonate (294 g) and then concentrated at 35° C. under reduced pressure until the weight of the toluene layer reached to 243 g. After cooling to −10° C., to the concentrate was added dropwise n-hexane (310 g) over 3 hrs. Deposited crystals was filtered and dried to give N-Boc-O-tosyl L-tyrosine methyl ester 4 (147 g, yield 92%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714157B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-a6cab9044cde4372969dcbfcb439f237 |
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| Source note | uspto-grants-2010_05 |
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