Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Alanine | HCID 5950 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-Tosyl-L-alanine | HCID 737622 | — |
Reaction Steps
L-alanine (100 g; 1.11 moles) was dissolved in 2.25 L of 1N sodium hydroxide (aq), cooled to 5° C. and stirred while a solution of p-toluenesulfonyl chloride (218 g; 1.11 moles) dissolved in 450 mL of toluene was added slowly. The mixture was stirred at ambient temperature for 20 hr. The layers were separated and the chilled aqueous layer acidified to pH 1 with concentrated hydrochloric acid. The white solid title compound was collected by filtration, washed with water and dried. Yield 178.5 g (66%) mp 134°-5° C. IR (CHCl3) cm-1 1726, 1340, 1165, 1095; 1H NMR (DMSO-D6) δ 1.20 (d, J=7, 3H), 2.40 (s, 3H), 3.85 (p, J=8, 1H), 6.4 (br s, 1H)(CO2), 7.41 (d, |JAB |=8, 2H) and 7.75 (d, |JAB |=8, 2H) [ center of pattern: 7.58; ΔVAB =20.49 Hz], 8.03 (br d, J=8, 1H)(NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04657855 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-b0c09ae2ca3f41dab3f76c1228b94f31 |
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| Source note | uspto-grants-1987_04 |
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