HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615349Generated: October 25, 2026
Succinic anhydride → HCID 12837158, compound
https://huagongshe.com/reaction/615349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (4R)-2-(2-hydroxyphenyl)-1,3-thiazolidine-4-carboxylic acid | HCID 2825745 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 12837158 | HCID 12837158 | 75.4% |
Reaction Steps
To a stirred solution of (4R)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid (4.5 g) and triethylamine (4.0 g) in acetone (100 ml), succinic anhydride (2.0 g) was added at room temperature, and stirred for 3 hours at the same temperature. The reaction mixture was concentrated in vacuo, and acidified with dilute hydrochloric acid. The separated oil was extracted with ethyl acetate, and the organic layer was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and evaporated in vacuo to give 4.9 g (75%) of the titled compound: mp 190°-191° C. (dec.) (ethyl acetate-methanol); [α]D27 +181.6° (c=1.0, methanol). IR (nujol, cm-1): 3210 (OH), 1720 (COOH), 1618 (CON), 1602 (aromatic), 1245, 1173, 940, 763. NMR (DMSO-6, δ): 2.0-2.7 (4H, m, --CH2CH2 --), 3.03 (1H, ABq (A part), d, J=11.0, 10.0 Hz, C5 --HA), 3.36 (1H, ABq (B part), d, J=11.0, 7.0 Hz, C5 --HB), 4.61 and 5.07 (1H, dd, J=10.0, 7.0 Hz and m, C4 --H), 6.36 (1H, s, C2 --H), 6.5-8.0 (4H, arom. H). TLC: Rf value* 0.35.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04499102 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-51b53ba6ac114adaa8d98b2efb8ff27c |
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| Source note | uspto-grants-1985_02 |
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