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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226869Generated: October 31, 2026

Formaldehyde → Methyl 4-chloro-3-(dimethylamino)benzo[b]thiophene-2-carboxylate

https://huagongshe.com/reaction/2226869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 3-amino-4-chloro-1-benzothiophene-2-carboxylateHCID 2818443—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductMethyl 4-chloro-3-(dimethylamino)benzo[b]thiophene-2-carboxylateHCID 18963790—

Reaction Steps

A mixture of methyl 3-amino-4-chlorobenzo[b]thiophene-2-carboxylate (1.7 g, 7.0 mmol) [Beck J. R., supra] and paraformaldehyde (2.0 g, 67 mmol) in 45 mL of acetic acid is treated in portions with sodium cyanoborohydride (2.0 g, 32 mmol). The mixture is stirred at room temperature for 24 hours, then diluted cautiously with 250 g of ice and water. Solid sodium carbonate is added until the mixture is slightly basic. After extraction with ethyl acetate, the combined organic layers are washed with brine, then dried (anhydrous sodium sulfate), and evaporated to provide methyl 4-chloro-3-(dimethylamino)benzo[b]thiophene-2-carboxylate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350748
Source datasetuspto-grants-1994_09
ORD IDord-c22f4b6d166f4ad583e4c3b8f6b48483
Source noteuspto-grants-1994_09